Our full list of 482 drug products tracked by the FDA, each
carrying one of the three statuses below. Search, sort, or filter the list — click a status
card to filter by status, or expand a row for package-level detail. Please note that the
list changes constantly and could contain errors.
Details
Generic Name
Company Name
Therapeutic Category
Date of Update
Status
Clonazepam Tablet
Teva Pharmaceuticals USA, Inc.
NeurologyPediatricPsychiatry
2026-10-23
Currently in Shortage
First posted by the FDA
2023-03-10
Presentations affected
6
Manufacturer contact
800-545-8800
Clonazepam, Tablet, .5 mg (NDC 0093-0832-01) Available
Clonazepam, Tablet, .5 mg (NDC 0093-0832-05) Available
Clonazepam, Tablet, 1 mg (NDC 0093-3212-01) Available
Clonazepam, Tablet, 1 mg (NDC 0093-3212-05) Available
Clonazepam, Tablet, 2 mg (NDC 0093-3213-01) Available
Clonazepam, Tablet, 2 mg (NDC 0093-3213-05) Available
Metformin Hydrochloride Tablet, Extended Release
Mylan Pharmaceuticals Inc., a Viatris Company
Endocrinology/Metabolism
2026-10-22
To Be Discontinued
First posted by the FDA
2026-10-22
Presentations affected
2
Manufacturer contact
800-796-9526
Metformin Hydrochloride, Tablet, Extended Release, 1000 mg (NDC 0378-6001-91)A business decision was made was discontinue manufacture of the drug product.
Metformin Hydrochloride, Tablet, Extended Release, 500 mg (NDC 0378-6002-91)A business decision was made was discontinue manufacture of the drug product.
Bupivacaine Hydrochloride and Epinephrine, Injection, 125 mg/50 mL (2.5 mg/mL) (NDC 0409-9043-01) Unavailable Other
Bupivacaine Hydrochloride and Epinephrine, Injection, 150 mg/30 mL (5 mg/mL) (NDC 0409-9045-17) Unavailable Other
Bupivacaine Hydrochloride And Epinephrine, Injection, 25 mg/10 mL (2.5 mg/mL) (NDC 0409-9042-01) Unavailable Other
Bupivacaine Hydrochloride And Epinephrine, Injection, 250 mg/50 mL (5 mg/mL) (NDC 0409-9046-01) Unavailable Other
Bupivacaine Hydrochloride And Epinephrine, Injection, 50 mg/10 mL (5 mg/mL) (NDC 0409-9045-01) Unavailable Other
Bupivacaine Hydrochloride And Epinephrine, Injection, 75 mg/30 mL (2.5 mg/mL) (NDC 0409-9042-17) Unavailable Other
Marcaine With Epinephrine, Injection, Marcaine with Epinephrine 1:200,000 as the bitartrate 125 mg/50 mL (2.5 mg/mL 1:200,000) (NDC 0409-1752-50) Limited Availability Other
Marcaine With Epinephrine, Injection, Marcaine with Epinephrine 1:200,000 as the bitartrate 150 mg/30 mL (5 mg/mL 1:200,000) (NDC 0409-1749-29) Available
Marcaine With Epinephrine, Injection, Marcaine with Epinephrine 1:200,000 as the bitartrate 25 mg/10 mL (2.5 mg/mL 1:200,000) (NDC 0409-1746-10) Available
Marcaine With Epinephrine, Injection, Marcaine with Epinephrine 1:200,000 as the bitartrate 250 mg/50 mL (5 mg/mL 1:200,000) (NDC 0409-1755-50) Available
Marcaine With Epinephrine, Injection, Marcaine with Epinephrine 1:200,000 as the bitartrate 50 mg/10 mL (5 mg/mL 1:200,000) (NDC 0409-1749-10) Available
Marcaine With Epinephrine, Injection, Marcaine with Epinephrine 1:200,000 as the bitartrate 75 mg/30 mL (2.5 mg/mL 1:200,000) (NDC 0409-1746-30) Available
Carboplatin Injection
Gland Pharma Limited
Oncology
2026-10-21
Currently in Shortage
First posted by the FDA
2023-04-28
Presentations affected
4
Manufacturer contact
Distributed by BPI Labs, LLC; Customer service number: (727) 471-0850 Ext 270
Carboplatin, Injection, 150mg/15mL (NDC 54288-165-01) Available Distributed by BPI Labs, LLC
Carboplatin, Injection, 450mg/45mL (NDC 54288-166-01) Limited Availability Demand increase for the drug
Carboplatin, Injection, 50mg/5mL (NDC 54288-164-01) Unavailable Discontinuation of the manufacture of the drug
Carboplatin, Injection, 600 mg/65 mL (NDC 54288-167-01) Limited Availability Demand increase for the drug
Clindamycin Phosphate Injection
Pfizer Inc.
Anti-Infective
2026-10-21
Currently in Shortage
First posted by the FDA
2023-03-21
Presentations affected
3
Manufacturer contact
800-533-4535
Cleocin Phosphate, Injection, Cleocin Phosphate 300 mg/2 mL (150 mg/mL) (NDC 0009-0870-26) Unavailable Other
More from the FDA
Cleocin Phosphate, Injection, Cleocin Phosphate 600 mg/4 mL (150 mg/mL) (NDC 0009-0775-26) Unavailable Other
More from the FDA
Cleocin Phosphate, Injection, Cleocin Phosphate 900 mg/6 mL (150 mg/mL) (NDC 0009-0902-18) Unavailable Other
More from the FDA
Clindamycin Phosphate Injection
Sandoz Inc.
Anti-Infective
2026-10-21
Currently in Shortage
First posted by the FDA
2023-03-21
Presentations affected
5
Manufacturer contact
800-525-8747
Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 12 mg/1 mL (NDC 0781-3289-09) Available
Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 12 mg/1 mL (NDC 72572-074-24) Available Civica Label
Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 18 mg/1 mL (NDC 0781-3290-09) Available
Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 18 mg/1 mL (NDC 72572-076-24) Available Civica Label
Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 6 mg/1 mL (NDC 0781-3288-09) Available
Dexmedetomidine Hydrochloride Injection
Gland Pharma Limited
Anesthesia
2026-10-21
Currently in Shortage
First posted by the FDA
2020-04-10
Presentations affected
3
Manufacturer contact
855-273-0154
Dexmedetomidine Hydrochloride, Injection, 200 ug/2 mL (NDC 66794-230-42) Available Marketed by Piramal Critical Care Inc.: 800-414-1901
Dexmedetomidine Hydrochloride, Injection, 4 ug/1 mL (NDC 43598-975-58) Available Distributed by DRL
Dexmedetomidine Hydrochloride, Injection, 4 ug/1 mL (NDC 43598-976-58) Available Distributed by DRL
Dexmedetomidine Hydrochloride Injection
Pfizer Inc.
Anesthesia
2026-10-21
Currently in Shortage
First posted by the FDA
2020-04-10
Presentations affected
14
Manufacturer contact
844-646-4398
Precedex, Injection, 1000 mcg/250 mL Glass Bottle NovaPlus (NDC 0409-2815-01) Available
Precedex, Injection, 1000 mcg/250 mL Single Dose Glass Bottle (NDC 0409-1434-01) Available
Precedex, Injection, 200 mcg/50 mL (4 mcg/mL) (NDC 0409-1454-20) Available
Precedex, Injection, 200 mcg/50 mL (4 mcg/mL) (NDC 0409-1660-50) Available
Precedex, Injection, 200 mcg/50 mL (4 mcg/mL) (NDC 0409-4596-20) Available
Precedex, Injection, 200 mcg/50 mL (NDC 0409-7838-24) Available
Precedex, Injection, 400 mcg/100 mL (4 mcg/mL) (NDC 0409-0155-02) Available
Precedex, Injection, 400 mcg/100 mL (4 mcg/mL) (NDC 0409-1174-10) Available
Precedex, Injection, 400 mcg/100 mL (4 mcg/mL) (NDC 0409-1596-10) Available
Precedex, Injection, 400 mcg/100 mL (NDC 0409-7853-24) Available
Precedex, Injection, 80 mcg/20 mL (4 mcg/mL) (NDC 0409-3301-10) Limited Availability Other
Precedex, Injection, 1000 mcg/250 mL (NDC 0409-7875-12) Available
Precedex, Injection, 80 mcg/20 mL (4 mcg/mL) (NDC 0409-1660-20) Available
Precedex, Injection, 200 mcg/2 mL (100 mcg/mL) (NDC 0409-1638-02) Available
Dextrose Monohydrate 50% Injection
Hospira, Inc., a Pfizer Company
Endocrinology/MetabolismGastroenterologyPediatric
2026-10-21
Currently in Shortage
First posted by the FDA
2022-01-13
Presentations affected
2
Manufacturer contact
844-646-4398
Dextrose Monohydrate 50%, Injection, 25 g/50 mL (NDC 0409-6648-02) Limited Availability Other
Dextrose Monohydrate 50%, Injection, 25 g/50 mL (NDC 0409-7517-16) Unavailable Other
Dobutamine Hydrochloride Injection
Hainan Poly Pharm. Co., Ltd.
CardiovascularPediatricRenal
2026-10-21
Currently in Shortage
First posted by the FDA
2017-11-06
Presentations affected
1
Manufacturer contact
Slate Run Pharmaceuticals, LLC: 844-529-8988
Dobutamine Hydrochloride, Injection, 250 mg/20 mL (NDC 70436-203-80) Available Distributed by Slate Run Pharmaceuticals, LLC, 1-844-529-8988
Dobutamine Hydrochloride Injection
Hospira, Inc., a Pfizer Company
CardiovascularPediatricRenal
2026-10-21
Currently in Shortage
First posted by the FDA
2017-11-06
Presentations affected
6
Manufacturer contact
844-646-4398
Dobutamine Hydrochloride In Dextrose 5% In Plastic Container, Injection, 1,000 mg/250mL (4 mg/mL) (NDC 0409-1100-10) Available
Dobutamine Hydrochloride In Dextrose 5% In Plastic Container, Injection, 250 mg/250mL (1 mg/mL) (NDC 0409-0025-10) Available
Dobutamine Hydrochloride In Dextrose 5% In Plastic Container, Injection, 500 mg/250mL (2 mg/mL) (NDC 0409-0151-10) Available
Sodium Acetate, Injection, 100 mEq/50 mL (2 mEq/mL) (NDC 0409-3299-05) Available
Sodium Acetate, Injection, 100 mEq/50 mL (2 mEq/mL) (NDC 0409-3299-26) Available
Sodium Acetate, Injection, 200 mEq/100 mL (2 mEq/mL) (NDC 0409-3299-06) Available
Sodium Acetate, Injection, 200 mEq/100 mL (2 mEq/mL) (NDC 0409-3299-25) Available
Sodium Acetate, Injection, 40 mEq/20 mL (2 mEq/mL) (NDC 0409-7299-25) Available
Sodium Acetate, Injection, 40 mEq/20 mL (2 mEq/mL) (NDC 0409-7299-73) Available
Sodium Bicarbonate Injection
Hospira, Inc., a Pfizer Company
Endocrinology/MetabolismGastroenterologyPediatric
2026-10-21
Currently in Shortage
First posted by the FDA
2017-03-01
Presentations affected
4
Manufacturer contact
844-646-4398
Sodium Bicarbonate, Injection, 2.5 mEq/5 mL (4.2%, 0.5 mEq/mL) (NDC 0409-5555-01) Limited Supply Available. Next Delivery and Estimated Recovery: June 2027 Other
Sodium Bicarbonate, Injection, 2.5 mEq/5 mL (4.2%, 0.5 mEq/mL) (NDC 0409-5555-02) Limited Availability Demand increase for the drug
Sodium Bicarbonate, Injection, 50 mEq/50 mL (8.4%, 1 mEq/mL) (NDC 0409-6625-14) Available
Sodium Bicarbonate, Injection, 50 mEq/50 mL (8.4%, 1 mEq/mL) (NDC 0409-6625-35) Unavailable Other
Sterile Water Injection
Hospira, Inc., a Pfizer Company
Other
2026-10-21
Currently in Shortage
First posted by the FDA
2021-11-23
Presentations affected
5
Manufacturer contact
844-646-4398
Bacteriostatic Water For Injection In Plastic Container, Injection, 1 mL/1 mL (NDC 0409-3977-03) Available
Sterile Water, Injection, 1 mL/1 mL (NDC 0409-4887-10) Available
Sterile Water, Injection, 1 mL/1 mL (NDC 0409-4887-20) Available
Sterile Water, Injection, 1 mL/1 mL (NDC 0409-4887-50) Available
Sterile Water, Injection, 1 mL/1 mL (NDC 0409-4887-99) Available
Sufentanil Citrate Injection
Hospira, Inc., a Pfizer Company
Analgesia/AddictionPediatric
2026-10-21
Currently in Shortage
First posted by the FDA
2022-05-03
Presentations affected
1
Manufacturer contact
844-646-4398
Sufentanil Citrate, Injection, 50 ug/1 mL (NDC 0409-3382-21) Limited Availability Other
Azacitidine Injection
Dr. Reddy's Laboratories, Inc.
Oncology
2026-10-20
Currently in Shortage
First posted by the FDA
2020-12-18
Presentations affected
1
Manufacturer contact
866-732-3952
Azacitidine, Injection, 100 mg (NDC 43598-305-62) Available Available to existing customers
Carboplatin Injection
Teyro Labs
Oncology
2026-10-20
Currently in Shortage
First posted by the FDA
2023-04-28
Presentations affected
4
Manufacturer contact
Natco Pharma USA LLC: (201)786-6500
Carboplatin, Injection, 150 mg/15 mL (NDC 69339-365-15) Available Wholesaler & Distributor through Marketing partner (Natco Pharma USA LLC)
Carboplatin, Injection, 450 mg/45 mL (NDC 69339-366-45) Available Wholesaler & Distributor through Marketing partner (Natco Pharma USA LLC)
Carboplatin, Injection, 50 mg/5 mL (NDC 69339-364-05) Available Wholesaler & Distributor through Marketing partner (Natco Pharma USA LLC)
Carboplatin, Injection, 600 mg/60 mL (NDC 69339-367-60) Available Wholesaler & Distributor through Marketing partner (Natco Pharma USA LLC)
Enoxaparin Sodium Injection
Sanofi-Aventis U.S. LLC
Hematology
2026-10-20
To Be Discontinued
First posted by the FDA
2026-10-20
Presentations affected
24
Manufacturer contact
800-631-1610
Enoxaparin Sodium, Injection, 100 mg/1 mL (NDC 0955-1010-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Enoxaparin Sodium, Injection, 120 mg/.8 mL (NDC 0955-1012-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Enoxaparin Sodium, Injection, 150 mg/1 mL (NDC 0955-1015-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Enoxaparin Sodium, Injection, 30 mg/.3 mL (NDC 0955-1003-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Enoxaparin Sodium, Injection, 300 mg/3 mL (NDC 0955-1016-01)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Enoxaparin Sodium, Injection, 40 mg/.4 mL (NDC 0955-1004-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Enoxaparin Sodium, Injection, 60 mg/.6 mL (NDC 0955-1006-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Enoxaparin Sodium, Injection, 80 mg/.8 mL (NDC 0955-1008-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 100 mg/1 mL (NDC 0075-0623-00)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 100 mg/1 mL (NDC 0075-8020-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 120 mg/.8 mL (NDC 0075-2912-01)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 120 mg/.8 mL (NDC 0075-8022-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 150 mg/1 mL (NDC 0075-2915-01)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 150 mg/1 mL (NDC 0075-8025-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 30 mg/.3 mL (NDC 0075-0624-30)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 30 mg/.3 mL (NDC 0075-8013-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 300 mg/3 mL (NDC 0075-0626-03)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 300 mg/3 mL (NDC 0075-8030-01)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 40 mg/.4 mL (NDC 0075-0620-40)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 40 mg/.4 mL (NDC 0075-8014-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 60 mg/.6 mL (NDC 0075-0621-60)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 60 mg/.6 mL (NDC 0075-8016-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 80 mg/.8 mL (NDC 0075-0622-80)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Lovenox, Injection, 80 mg/.8 mL (NDC 0075-8018-10)Discontinuation of the manufacture of the drug for the U.S. market. This decision is not related to product safety or quality concerns. FDA-approved generic enoxaparin products and other treatment options are available. Remaining inventory may continue to be available through wholesalers and other distribution channels until existing supplies are depleted. Availability may vary by presentation with last lot expected to expire in March 2029.
Leuprolide Acetate Injection
Amneal Pharmaceuticals
Oncology
2026-10-20
To Be Discontinued
First posted by the FDA
2026-10-20
Presentations affected
1
Manufacturer contact
866.525.7270
Leuprolide Acetate, Injection, 14 mg/2.8 mL (1 mg/0.2 mL) (NDC 70121-2537-6)A business decision was made to discontinue manufacture of the drug.
Dextrose Monohydrate 70%, Injection, 70 g/100 mL (NDC 0264-7387-50) Available
Etomidate Injection
Eugia US LLC
Anesthesia
2026-10-19
Currently in Shortage
First posted by the FDA
2022-10-05
Presentations affected
2
Manufacturer contact
888-238-7880
Etomidate, Injection, 20 mg/10 mL (NDC 55150-221-10) Unavailable Demand increase for the drug
Etomidate, Injection, 40 mg/20 mL (NDC 55150-222-20) Unavailable Demand increase for the drug
Etomidate Injection
Mylan Institutional, a Viatris Company
Anesthesia
2026-10-19
Currently in Shortage
First posted by the FDA
2022-10-05
Presentations affected
2
Manufacturer contact
800-796-9526
Etomidate, Injection, 2 mg/1 mL (NDC 67457-902-10) Unavailable Demand increase for the drug
Etomidate, Injection, 2 mg/1 mL (NDC 67457-903-20) Available
Furosemide Injection
Eugia US LLC
Cardiovascular
2026-10-19
Currently in Shortage
First posted by the FDA
2020-04-07
Presentations affected
3
Manufacturer contact
888-238-7880
Furosemide, Injection, 100 mg/10 mL (NDC 55150-324-25) Available Check wholesalers for inventory
Furosemide, Injection, 20 mg/2 mL (NDC 55150-322-25) Unavailable Demand increase for the drug
Furosemide, Injection, 40 mg/4 mL (NDC 55150-323-25) Available Check wholesalers for inventory
Heparin Sodium Injection
B. Braun Medical Inc.
Hematology
2026-10-19
Currently in Shortage
First posted by the FDA
2017-11-14
Presentations affected
2
Manufacturer contact
800-227-2862
Heparin Sodium 1,000 Units In Sodium Chloride 0.9% In Plastic Container, Injection, 200 [USP'U]/100 mL (NDC 0264-9872-10) Limited Availability Other
Heparin Sodium 2,000 Units in Sodium Chloride 0.9% in Plastic Container, Injection, 200 [USP'U]/100 mL (NDC 0264-9872-00) Limited Availability Other
Hydroxocobalamin Injection
BTG International Inc.
Other
2026-10-19
Currently in Shortage
First posted by the FDA
2024-11-04
Presentations affected
1
Manufacturer contact
1 877 377 3784
Cyanokit, Injection, 5 g/250mL (NDC 50633-310-11) Limited Availability Other
More from the FDA
Lamivudine Tablet
ViiV Healthcare Company
Antiviral
2026-10-19
To Be Discontinued
First posted by the FDA
2026-10-19
Presentations affected
2
Manufacturer contact
800-844-8872
Epivir, Tablet, 150 mg (NDC 49702-203-18)The anticipated date that ViiV will cease distribution of the products is approximately April 15, 2027; Discontinuation of the manufacture of the drug
Epivir, Tablet, 300 mg (NDC 49702-204-13)The anticipated date that ViiV will cease distribution of the products is approximately April 15, 2027; Discontinuation of the manufacture of the drug
Lidocaine Hydrochloride Injection
B. Braun Medical Inc.
Cardiovascular
2026-10-19
Currently in Shortage
First posted by the FDA
2017-10-25
Presentations affected
3
Manufacturer contact
800-227-2862
Lidocaine Hydrochloride And Dextrose, Injection, 5 g/100 mL; .4 g/100 mL (NDC 0264-9594-10) Available
Lidocaine Hydrochloride And Dextrose, Injection, 5 g/100 mL; .4 g/100 mL (NDC 0264-9594-20) Available
Lidocaine Hydrochloride And Dextrose, Injection, 5 g/100 mL; .8 g/100 mL (NDC 0264-9598-20) Available
Lidocaine Hydrochloride Injection
Eugia US LLC
Anesthesia
2026-10-19
Currently in Shortage
First posted by the FDA
2018-02-20
Presentations affected
11
Manufacturer contact
888-238-7880
Lidocaine Hydrochloride, Injection, 10 mg/1 mL (NDC 55150-159-74) Unavailable Demand increase for the drug
Lidocaine Hydrochloride, Injection, 10 mg/1 mL (NDC 55150-161-02) Available Check wholesalers for inventory
Lidocaine Hydrochloride, Injection, 10 mg/1 mL (NDC 55150-162-05) Available Check wholesalers for inventory
Lidocaine Hydrochloride, Injection, 10 mg/1 mL (NDC 55150-163-30) Available Check wholesalers for inventory
Lidocaine Hydrochloride, Injection, 10 mg/mL (NDC 55150-251-10) Available Check wholesalers for inventory
Lidocaine Hydrochloride, Injection, 10 mg/mL (NDC 55150-252-20) Unavailable Demand increase for the drug
Lidocaine Hydrochloride, Injection, 20 mg/1 mL (NDC 55150-165-05) Unavailable Demand increase for the drug
Lidocaine Hydrochloride, Injection, 20 mg/mL (NDC 55150-164-02) Available Check wholesalers for inventory
Lidocaine Hydrochloride, Injection, 20 mg/mL (NDC 55150-254-10) Unavailable Demand increase for the drug
Lidocaine Hydrochloride, Injection, 20 mg/mL (NDC 55150-255-20) Available Check wholesalers for inventory
Lidocaine Hydrochloride, Injection, 20 mg/mL (NDC 55150-256-50) Unavailable Demand increase for the drug
Lisdexamfetamine Dimesylate Capsule
Mylan Pharmaceuticals Inc., a Viatris Company
Psychiatry
2026-10-19
Currently in Shortage
First posted by the FDA
2023-07-14
Presentations affected
7
Manufacturer contact
800-796-9526
Lisdexamfetamine Dimesylate, Capsule, 10 mg (NDC 0378-6854-77) Available
Lisdexamfetamine Dimesylate, Capsule, 20 mg (NDC 0378-6855-77) Available
Lisdexamfetamine Dimesylate, Capsule, 30 mg (NDC 0378-6856-77) Available
Lisdexamfetamine Dimesylate, Capsule, 40 mg (NDC 0378-6857-77) Available
Lisdexamfetamine Dimesylate, Capsule, 50 mg (NDC 0378-6858-77) Available
Lisdexamfetamine Dimesylate, Capsule, 60 mg (NDC 0378-6859-77) Available
Lisdexamfetamine Dimesylate, Capsule, 70 mg (NDC 0378-6860-77) Available
Lisdexamfetamine Dimesylate Capsule
Sun Pharmaceutical Industries, Inc.
Psychiatry
2026-10-19
Currently in Shortage
First posted by the FDA
2023-07-14
Presentations affected
7
Manufacturer contact
800-818-4555
Lisdexamfetamine Dimesylate, Capsule, 10 mg (NDC 57664-046-88) Limited Availability Other
Lisdexamfetamine Dimesylate, Capsule, 20 mg (NDC 57664-047-88) Limited Availability Other
Lisdexamfetamine Dimesylate, Capsule, 30 mg (NDC 57664-048-88) Limited Availability Other
Lisdexamfetamine Dimesylate, Capsule, 40 mg (NDC 57664-049-88) Limited Availability Other
Lisdexamfetamine Dimesylate, Capsule, 50 mg (NDC 57664-050-88) Limited Availability Other
Lisdexamfetamine Dimesylate, Capsule, 60 mg (NDC 57664-051-88) Limited Availability Other
Lisdexamfetamine Dimesylate, Capsule, 70 mg (NDC 57664-052-88) Limited Availability Other
Lisdexamfetamine Dimesylate Tablet, Chewable
Sun Pharmaceutical Industries, Inc.
Psychiatry
2026-10-19
Currently in Shortage
First posted by the FDA
2023-07-14
Presentations affected
6
Manufacturer contact
800-818-4555
Lisdexamfetamine Dimesylate, Tablet, Chewable, 10 mg (NDC 57664-083-88) Available
Lisdexamfetamine Dimesylate, Tablet, Chewable, 20 mg (NDC 57664-084-88) Available
Lisdexamfetamine Dimesylate, Tablet, Chewable, 30 mg (NDC 57664-085-88) Available
Lisdexamfetamine Dimesylate, Tablet, Chewable, 40 mg (NDC 57664-086-88) Available
Lisdexamfetamine Dimesylate, Tablet, Chewable, 50 mg (NDC 57664-087-88) Available
Lisdexamfetamine Dimesylate, Tablet, Chewable, 60 mg (NDC 57664-088-88) Available
Aminosyn II 10% In Plastic Container, Injection, 0.1 (NDC 0990-7172-17) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Aminosyn II 15% In Plastic Container, Injection, 0.15 (NDC 0990-7171-17) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Aminosyn-PF 10%, Injection, 0.1 (NDC 0990-4179-05) Unavailable Shortage of an active ingredient
Aminosyn-PF 7%, Injection, 0.07 (NDC 0990-4178-03) Unavailable Shortage of an active ingredient
Dextrose 10% In Plastic Container, Injection, 10 g/100 mL (NDC 0990-7930-02) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 10% In Plastic Container, Injection, 10 g/100 mL (NDC 0990-7930-03) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 10% In Plastic Container, Injection, 10 g/100 mL (NDC 0990-7930-09) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 10% In Plastic Container, Injection, 10 g/100 mL (NDC 0990-7938-19) Unavailable Discontinuation of the manufacture of the drug
Dextrose 5% In Plastic Container, Injection, 5 g/100 mL (NDC 0990-7922-02) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 5% In Plastic Container, Injection, 5 g/100 mL (NDC 0990-7922-03) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 5% In Plastic Container, Injection, 5 g/100 mL (NDC 0990-7922-09) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 5% In Plastic Container, Injection, 5 g/100 mL (NDC 0990-7922-55) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 5% In Plastic Container, Injection, 5 g/100 mL (NDC 0990-7922-61) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 5% In Plastic Container, Injection, 5 g/100 mL (NDC 0990-7923-13) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 5% In Plastic Container, Injection, 5 g/100 mL (NDC 0990-7923-20) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 5% In Plastic Container, Injection, 5 g/100 mL (NDC 0990-7923-23) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 5% In Plastic Container, Injection, 5 g/100 mL (NDC 0990-7923-36) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose 5% In Plastic Container, Injection, 5 g/100 mL (NDC 0990-7923-37) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dextrose Monohydrate 50% Injection
Amphastar Pharmaceuticals, Inc.
Endocrinology/MetabolismGastroenterologyPediatric
2026-10-16
Currently in Shortage
First posted by the FDA
2022-01-13
Presentations affected
1
Manufacturer contact
800-423-4136
Dextrose Monohydrate 50%, Injection, 25 g/50 mL (NDC 76329-3302-1) Limited Availability Demand increase for the drug
DEXTROSE 70% IN PLASTIC CONTAINER, Injection, 70 g/100 mL (NDC 0990-7120-07) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
DEXTROSE 70% IN PLASTIC CONTAINER, Injection, 70 g/100 mL (NDC 0990-7918-19) Available This product is distributed by ICU Medical. For questions regarding this product, please contact ICU Medical.
Dobutamine Hydrochloride Injection
Baxter Healthcare
CardiovascularPediatricRenal
2026-10-16
Currently in Shortage
First posted by the FDA
2017-11-06
Presentations affected
3
Manufacturer contact
888-229-0001
Dobutamine Hydrochloride In Dextrose 5% In Plastic Container, Injection, 100 mg/100 mL (NDC 0338-1073-02) Available
Dobutamine Hydrochloride In Dextrose 5% In Plastic Container, Injection, 200 mg/100 mL (NDC 0338-1075-02) Available
Dobutamine Hydrochloride In Dextrose 5% In Plastic Container, Injection, 400 mg/100 mL (NDC 0338-1077-02) Available
Dopamine Hydrochloride Injection
Baxter Healthcare
Cardiovascular
2026-10-16
Currently in Shortage
First posted by the FDA
2017-11-06
Presentations affected
4
Manufacturer contact
888-229-0001
Dopamine Hydrochloride In Dextrose 5% In Plastic Container, Injection, 160 mg/100 mL (NDC 0338-1007-02) Available
Dopamine Hydrochloride In Dextrose 5% In Plastic Container, Injection, 160 mg/100 mL (NDC 0338-1007-03) Available
Dopamine Hydrochloride In Dextrose 5% In Plastic Container, Injection, 80 mg/100 mL (NDC 0338-1005-02) Available
Dopamine Hydrochloride In Dextrose 5% In Plastic Container, Injection, 80 mg/100 mL (NDC 0338-1005-03) Available
Furosemide Injection
Baxter Healthcare
Cardiovascular
2026-10-16
Currently in Shortage
First posted by the FDA
2020-04-07
Presentations affected
3
Manufacturer contact
888-229-0001
Furosemide, Injection, 10 mg/1 mL (NDC 36000-282-25) Available
Furosemide, Injection, 10 mg/1 mL (NDC 36000-283-25) Available
Furosemide, Injection, 10 mg/1 mL (NDC 36000-284-25) Available
Heparin Sodium Injection
Baxter Healthcare
Hematology
2026-10-16
Currently in Shortage
First posted by the FDA
2017-11-14
Presentations affected
2
Manufacturer contact
888-229-0001
Heparin Sodium In Sodium Chloride, Injection, 200 [USP'U]/100 mL (NDC 0338-0431-03) Limited Availability Demand increase for the drug
Heparin Sodium In Sodium Chloride, Injection, 200 [USP'U]/100 mL (NDC 0338-0433-04) Available
Ifosfamide Injection
Baxter Healthcare
OncologyPediatric
2026-10-16
Currently in Shortage
First posted by the FDA
2026-06-12
Presentations affected
4
Manufacturer contact
888-229-0001
IFEX, Injection, 1 g/20 mL (NDC 0338-3991-01) Available
IFEX, Injection, 3 g/60 mL (NDC 0338-3993-01) Unavailable Requirements related to complying with good manufacturing practices
Ifosfamide, Injection, 1 g/20 mL (NDC 10019-925-01) Available
Ifosfamide, Injection, 3 g/60 mL (NDC 10019-926-02) Available
Ketorolac Tromethamine Injection
Baxter Healthcare
Analgesia/Addiction
2026-10-16
Currently in Shortage
First posted by the FDA
2018-06-06
Presentations affected
2
Manufacturer contact
888-229-0001
Ketorolac Tromethamine, Injection, 15 mg/1 mL (NDC 0338-0069-10) Unavailable Demand increase for the drug
Ketorolac Tromethamine, Injection, 30 mg/1 mL (NDC 0338-0072-25) Available
Lidocaine Hydrochloride Injection
Amphastar Pharmaceuticals, Inc.
AnesthesiaPediatric
2026-10-16
Currently in Shortage
First posted by the FDA
2012-02-22
Presentations affected
1
Manufacturer contact
800-423-4136
Lidocaine Hydrochloride, Injection, 20 mg/1 mL (NDC 76329-3390-1) Available
Lidocaine Hydrochloride Injection
Baxter Healthcare
Cardiovascular
2026-10-16
Currently in Shortage
First posted by the FDA
2017-10-25
Presentations affected
2
Manufacturer contact
888-229-0001
Lidocaine Hydrochloride And Dextrose, Injection, 4 mg/1 mL (NDC 0338-0409-03) Available
Lidocaine Hydrochloride And Dextrose, Injection, 8 mg/1 mL (NDC 0338-0411-02) Available
Sterile Water In Plastic Container, Irrigant, 1 mL/1 mL (NDC 0990-6139-03) Unavailable Discontinuation of the manufacture of the drug
More from the FDA
Sterile Water In Plastic Container, Irrigant, 1 mL/1 mL (NDC 0990-6139-22) Unavailable Discontinuation of the manufacture of the drug
More from the FDA
Sterile Water In Plastic Container, Irrigant, 1 mL/1 mL (NDC 0990-7139-09) Unavailable Discontinuation of the manufacture of the drug
More from the FDA
Sterile Water In Plastic Container, Irrigant, 1 mL/1 mL (NDC 0990-7139-36) Unavailable Discontinuation of the manufacture of the drug
More from the FDA
Technetium TC-99M Pyrophosphate Kit Injection
Curium US LLC
Medical Imaging
2026-10-16
Currently in Shortage
First posted by the FDA
2023-12-27
Presentations affected
1
Manufacturer contact
888-744-1414
Technescan PYP, Injection, 11.9 mg/10 mL; 3.2 mg/10 mL (NDC 69945-094-20) Limited Availability Shortage of an active ingredient
Vigabatrin Tablet
Hikma Pharmaceuticals USA, Inc.
Neurology
2026-10-16
To Be Discontinued
First posted by the FDA
2026-10-16
Presentations affected
1
Manufacturer contact
800-631-2174
Vigabatrin, Tablet, 500 mg (NDC 0054-0652-25)The decision to discontinue this drug product was due to a business decision and not due to any reasons of safety or effectiveness.
See Related Information section below for customer service information
Dexmedetomidine Hydrochloride, Injection, 200 mcg/2 mL (NDC 83634-600-02)Discontinuation of the manufacture of the drug; Distributed by Avenacy; Contact information: 877-283-6229
Dopamine Hydrochloride Injection
Hikma Pharmaceuticals USA, Inc.
Cardiovascular
2026-10-14
Currently in Shortage
First posted by the FDA
2017-11-06
Presentations affected
2
Manufacturer contact
800-631-2174
Dopamine Hydrochloride, Injection, 40 mg/1 mL (NDC 0143-9252-25) Unavailable Demand increase for the drug
Dopamine Hydrochloride, Injection, 40 mg/1 mL (NDC 0143-9254-25) Unavailable Demand increase for the drug
Etomidate Injection
Hikma Pharmaceuticals USA, Inc.
Anesthesia
2026-10-14
Currently in Shortage
First posted by the FDA
2022-10-05
Presentations affected
6
Manufacturer contact
800-631-2174
Etomidate, Injection, 2 mg/1 mL (NDC 0143-9310-10) Available Novaplus label
Etomidate, Injection, 2 mg/1 mL (NDC 0143-9311-10) Available Novaplus label
Etomidate, Injection, 2 mg/1 mL (NDC 0143-9506-10) Available Additional product will be made available as it is released.
Etomidate, Injection, 2 mg/1 mL (NDC 0143-9507-10) Available Additional product will be made available as it is released.
Etomidate, Injection, 2 mg/1 mL (NDC 72572-160-10) Available Distributed by Civica
Etomidate, Injection, 2 mg/1 mL (NDC 72572-161-10) Available Distributed by Civica
Everolimus Tablet
Par Health, USA LLC
Transplant
2026-10-14
To Be Discontinued
First posted by the FDA
2026-10-14
Presentations affected
4
Manufacturer contact
800-828-9393
Everolimus, Tablet, .25 mg (NDC 49884-158-02)A business decision was made to withdraw from sale.
Everolimus, Tablet, .5 mg (NDC 49884-159-02)A business decision was made to withdraw from sale.
Everolimus, Tablet, .75 mg (NDC 49884-160-02)A business decision was made to withdraw from sale.
Everolimus, Tablet, 1 mg (NDC 49884-283-02)A business decision was made to withdraw from sale.
Fentanyl Citrate Injection
Hikma Pharmaceuticals USA, Inc.
Analgesia/AddictionPediatric
2026-10-14
Currently in Shortage
First posted by the FDA
2023-12-20
Presentations affected
8
Manufacturer contact
800-631-2174
Fentanyl Citrate, Injection, 50 mcg/1 mL (NDC 0641-6027-25) Available Additional lots will be scheduled for manufacturing to meet demand. Product will be made available as it is released.
Fentanyl Citrate, Injection, 50 mcg/1 mL (NDC 0641-6028-25) Available Additional lots will be scheduled for manufacturing to meet demand. Product will be made available as it is released.
Fentanyl Citrate, Injection, 50 mcg/1 mL (NDC 0641-6029-25) Available Additional lots will be scheduled for manufacturing to meet demand. Product will be made available as it is released.
Fentanyl Citrate, Injection, 50 mcg/1 mL (NDC 0641-6030-01) Available Additional lots will be scheduled for manufacturing to meet demand. Product will be made available as it is released.
Fentanyl Citrate, Injection, 50 mcg/1 mL (NDC 0641-6247-25) Available Additional lots will be scheduled for manufacturing to meet demand. Product will be made available as it is released.
Fentanyl Citrate, Injection, 50 ug/1 mL (NDC 0641-6024-10) Unavailable Other
Fentanyl Citrate, Injection, 50 ug/1 mL (NDC 0641-6025-10) Unavailable Other
Fentanyl Citrate, Injection, 50 ug/1 mL (NDC 0641-6026-05) Unavailable Other
Furosemide Oral Solution
Hikma Pharmaceuticals USA, Inc.
Cardiovascular
2026-10-14
Currently in Shortage
First posted by the FDA
2026-03-31
Presentations affected
3
Manufacturer contact
800-631-2174
Furosemide, Oral Solution, 10 mg/1 mL (NDC 0054-3294-46) Available
Furosemide, Oral Solution, 10 mg/1 mL (NDC 0054-3294-50) Limited Availability Shortage of an inactive ingredient component
Furosemide, Oral Solution, 40 mg/5 mL (NDC 0054-3298-63) Available Shortage of an inactive ingredient component
Hydromorphone Hydrochloride Injection
Hikma Pharmaceuticals USA, Inc.
Analgesia/Addiction
2026-10-14
Currently in Shortage
First posted by the FDA
2017-11-01
Presentations affected
2
Manufacturer contact
800-631-2174
Hydromorphone Hydrochloride, Injection, 2 mg/1 mL (NDC 0641-0121-25) Available Additional lots are scheduled for manufacturing to meet demand. Product will be made available as it is released.
Hydromorphone Hydrochloride, Injection, 2 mg/1 mL (NDC 0641-6254-01) Unavailable Demand increase for the drug
Ifosfamide Injection
Hikma Pharmaceuticals USA, Inc.
OncologyPediatric
2026-10-14
Currently in Shortage
First posted by the FDA
2026-06-12
Presentations affected
2
Manufacturer contact
800-631-2174
Ifosfamide, Injection, 50 mg/1 mL (NDC 0143-9530-01) Unavailable Demand increase for the drug
Ifosfamide, Injection, 50 mg/1 mL (NDC 0143-9531-01) Unavailable Demand increase for the drug
Ketorolac Tromethamine Injection
Hikma Pharmaceuticals USA, Inc.
Analgesia/Addiction
2026-10-14
Currently in Shortage
First posted by the FDA
2018-06-06
Presentations affected
3
Manufacturer contact
800-631-2174
Ketorolac Tromethamine, Injection, 15 mg/1 mL (NDC 0641-6041-25) Unavailable Other
Ketorolac Tromethamine, Injection, 30 mg/1 mL (NDC 0641-6042-25) Unavailable Other
Ketorolac Tromethamine, Injection, 30 mg/1 mL (NDC 0641-6043-25) Unavailable Other
Lidocaine Hydrochloride Injection
Hikma Pharmaceuticals USA, Inc.
Anesthesia
2026-10-14
Currently in Shortage
First posted by the FDA
2018-06-13
Presentations affected
4
Manufacturer contact
800-631-2174
Lidocaine Hydrochloride, Injection, 10 mg/1 mL (NDC 0143-9577-10) Available Additional lots are scheduled for manufacturing to meet demand. Product will be made available as it is released.
Lidocaine Hydrochloride, Injection, 20 mg/1 mL (NDC 0143-9575-10) Available Additional lots are scheduled for manufacturing to meet demand. Product will be made available as it is released.
Lidocaine Hydrochloride, Preservative Free, Injection, 10 mg/1 mL (NDC 0143-9595-25) Unavailable Demand increase for the drug
Lidocaine Hydrochloride, Preservative Free, Injection, 20 mg/1 mL (NDC 0143-9594-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Liraglutide Injection
Hikma Pharmaceuticals USA, Inc.
Endocrinology/Metabolism
2026-10-14
Currently in Shortage
First posted by the FDA
2023-07-18
Presentations affected
2
Manufacturer contact
800-631-2174
Liraglutide, Injection, 6 mg/1 mL (NDC 0143-9144-02) Available
Liraglutide, Injection, 6 mg/1 mL (NDC 0143-9144-03) Available
Lisdexamfetamine Dimesylate Capsule
Hikma Pharmaceuticals USA, Inc.
Psychiatry
2026-10-14
Currently in Shortage
First posted by the FDA
2023-07-14
Presentations affected
7
Manufacturer contact
800-631-2174
Lisdexamfetamine Dimesylate, Capsule, 20 mg (NDC 0054-0370-25) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 30 mg (NDC 0054-0371-25) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 40 mg (NDC 0054-0372-25) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 50 mg (NDC 0054-0373-25) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 60 mg (NDC 0054-0374-25) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 70 mg (NDC 0054-0375-25) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 10 mg (NDC 0054-0660-25) Limited Availability Shortage of an active ingredient
Lorazepam Injection
Hikma Pharmaceuticals USA, Inc.
Neurology
2026-10-14
Currently in Shortage
First posted by the FDA
2018-05-03
Presentations affected
8
Manufacturer contact
800-631-2174
Ativan, Injection, 2 mg/1 mL (NDC 0641-6000-10) Unavailable Other
Ativan, Injection, 2 mg/1 mL (NDC 0641-6001-25) Limited Availability Demand increase for the drug
Ativan, Injection, 4 mg/1 mL (NDC 0641-6002-10) Unavailable Other
Ativan, Injection, 4 mg/1 mL (NDC 0641-6003-25) Limited Availability Demand increase for the drug
Lorazepam, Injection, 2 mg/1 mL (NDC 0641-6044-25) Limited Availability Demand increase for the drug
Lorazepam, Injection, 2 mg/1 mL (NDC 0641-6046-10) Unavailable Other
Lorazepam, Injection, 4 mg/1 mL (NDC 0641-6045-25) Limited Availability Demand increase for the drug
Lorazepam, Injection, 4 mg/1 mL (NDC 0641-6047-10) Unavailable Other
Meperidine Hydrochloride Injection
Hikma Pharmaceuticals USA, Inc.
Analgesia/Addiction
2026-10-14
Currently in Shortage
First posted by the FDA
2025-05-30
Presentations affected
3
Manufacturer contact
800-631-2174
Meperidine Hydrochloride, Injection, 100 mg/1 mL (NDC 0641-6054-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Meperidine Hydrochloride, Injection, 25 mg/1 mL (NDC 0641-6052-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Meperidine Hydrochloride, Injection, 50 mg/1 mL (NDC 0641-6053-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Methotrexate Sodium Injection
Hikma Pharmaceuticals USA, Inc.
OncologyRheumatology
2026-10-14
Currently in Shortage
First posted by the FDA
2023-03-13
Presentations affected
2
Manufacturer contact
800-631-2174
Methotrexate, Preservative Free, Injection, 1 g (NDC 0143-9830-01) Unavailable Demand increase for the drug
Methotrexate, Preservative Free, Injection, 25 mg/1 mL (NDC 0143-9519-10) Unavailable Demand increase for the drug
Midazolam Hydrochloride Injection
Hikma Pharmaceuticals USA, Inc.
AnesthesiaNeurology
2026-10-14
Currently in Shortage
First posted by the FDA
2020-04-02
Presentations affected
5
Manufacturer contact
800-631-2174
Midazolam Hydrochloride, Injection, 1 mg/1 mL (NDC 0641-6056-10) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Midazolam Hydrochloride, Injection, 1 mg/1 mL (NDC 0641-6057-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Midazolam Hydrochloride, Injection, 1 mg/1 mL (NDC 0641-6059-01) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Midazolam Hydrochloride, Injection, 5 mg/1 mL (NDC 0641-6060-10) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Midazolam Hydrochloride, Injection, 5 mg/1 mL (NDC 0641-6061-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Morphine Sulfate Injection
Hikma Pharmaceuticals USA, Inc.
Analgesia/Addiction
2026-10-14
Currently in Shortage
First posted by the FDA
2017-11-03
Presentations affected
7
Manufacturer contact
800-631-2174
Duramorph, Injection, .5 mg/1 mL (NDC 0641-6020-10) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Duramorph, Injection, 1 mg/1 mL (NDC 0641-6019-10) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Infumorph 200 (Preservative-Free Morphine Sulfate Sterile Solution), Injection, 10 mg/1 mL (NDC 0641-6039-01) Unavailable Demand increase for the drug
Infumorph 500 (Preservative-Free Morphine Sulfate Sterile Solution), Injection, 25 mg/1 mL (NDC 0641-6040-01) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Morphine Sulfate, Injection, 10 mg/1 mL (NDC 0641-6127-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Morphine Sulfate, Injection, 4 mg/1 mL (NDC 0641-6125-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Morphine Sulfate, Injection, 8 mg/1 mL (NDC 0641-6126-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Phenergan, Injection, 25 mg/1 mL (NDC 0641-6082-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Phenergan, Injection, 25 mg/1 mL (NDC 0641-6084-25) Unavailable Other
Phenergan, Injection, 50 mg/1 mL (NDC 0641-6083-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Phenergan, Injection, 50 mg/1 mL (NDC 0641-6085-25) Unavailable Other
Promethazine Hydrochloride, Injection, 25 mg/1 mL (NDC 0641-0928-25) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Promethazine Hydrochloride, Injection, 25 mg/1 mL (NDC 0641-1495-35) Unavailable Demand increase for the drug
Promethazine Hydrochloride, Injection, 50 mg/1 mL (NDC 0641-0929-25) Unavailable Demand increase for the drug
Promethazine Hydrochloride, Injection, 50 mg/1 mL (NDC 0641-1496-35) Available Additional lots are scheduled to be manufactured. Product will be made available as it is released.
Propranolol Hydrochloride Injection
Hikma Pharmaceuticals USA, Inc.
Cardiovascular
2026-10-14
Currently in Shortage
First posted by the FDA
2023-10-31
Presentations affected
1
Manufacturer contact
800-631-2174
Propranolol Hydrochloride, Injection, 1 mg/1 mL (NDC 0143-9872-10) Unavailable Shortage of an active ingredient
Remifentanil Hydrochloride Injection
Hikma Pharmaceuticals USA, Inc.
Analgesia/Addiction
2026-10-14
Currently in Shortage
First posted by the FDA
2022-06-28
Presentations affected
3
Manufacturer contact
800-631-2174
Remifentanil Hydrochloride, Injection, 1 mg per vial (NDC 0143-9391-10) Unavailable Demand increase for the drug
Remifentanil Hydrochloride, Injection, 2 mg per vial (NDC 0143-9392-10) Unavailable Demand increase for the drug
Remifentanil Hydrochloride, Injection, 5 mg per vial (NDC 0143-9393-10) Unavailable Demand increase for the drug
Rocuronium Bromide Injection
Hikma Pharmaceuticals USA, Inc.
Anesthesia
2026-10-14
Currently in Shortage
First posted by the FDA
2023-02-15
Presentations affected
2
Manufacturer contact
800-631-2174
Rocuronium Bromide, Injection, 10 mg/1 mL (NDC 0143-9250-10) Available Additional lots will be available. Product will be made available as it is released.
Rocuronium Bromide, Injection, 10 mg/1 mL (NDC 0143-9251-10) Available Additional lots will be available. Product will be made available as it is released.
Sodium Acetate, Injection, 100 mEq/50mL (2 mEq/mL) (NDC 0641-6262-01) Available Additional lots will be available. Product will be made available as it is released.
Sodium Acetate, Injection, 40 mEq/20mL (2 mEq/mL) (NDC 0641-6261-01) Available Additional lots will be available. Product will be made available as it is released.
Sterile Water Injection
Hikma Pharmaceuticals USA, Inc.
Other
2026-10-14
Currently in Shortage
First posted by the FDA
2021-11-23
Presentations affected
1
Manufacturer contact
800-631-2174
Sterile Water, Injection, 1 mL/1 mL (NDC 0641-6147-10) Unavailable Demand increase for the drug
Sufentanil Citrate Injection
Hikma Pharmaceuticals USA, Inc.
Analgesia/AddictionPediatric
2026-10-14
Currently in Shortage
First posted by the FDA
2022-05-03
Presentations affected
3
Manufacturer contact
800-631-2174
Sufentanil Citrate, Injection, 50 mcg/1 mL (NDC 17478-050-01) Unavailable Other
Sufentanil Citrate, Injection, 50 mcg/1 mL (NDC 17478-050-02) Unavailable Other
Sufentanil Citrate, Injection, 50 mcg/1 mL (NDC 17478-050-05) Unavailable Other
Valproate Sodium Injection
Hikma Pharmaceuticals USA, Inc.
Neurology
2026-10-14
Currently in Shortage
First posted by the FDA
2020-12-30
Presentations affected
1
Manufacturer contact
800-631-2174
Valproate Sodium, Injection, 500 mg/5 mL (NDC 0143-9785-10) Available Additional lots will be available. Product will be made available as it is released.
Zanosar, Powder, For Solution, 1 g/10 mL (NDC 68118-100-01) Available
More from the FDA
Dexmedetomidine Hydrochloride Injection
Accord Healthcare Inc.
Anesthesia
2026-09-15
Currently in Shortage
First posted by the FDA
2020-04-10
Presentations affected
2
Manufacturer contact
866-941-7875, option 2
Dexmedetomidine Hydrochloride, Injection, 100 ug/1 mL (NDC 16729-239-93) Unavailable Discontinuation of the manufacture of the drug
More from the FDA
Dexmedetomidine Hydrochloride, Injection, 100 ug/1 mL (NDC 16729-432-93) Unavailable Discontinuation of the manufacture of the drug
Flurazepam Hydrochloride Capsule
Chartwell Molecular Holdings LLC
NeurologyOncologyOther
2026-09-15
Currently in Shortage
First posted by the FDA
2022-08-03
Presentations affected
4
Manufacturer contact
845-268-5000 Ext. 510
Flurazepam Hydrochloride, Capsule, 15 mg (NDC 62135-736-30) Available
Flurazepam Hydrochloride, Capsule, 15 mg (NDC 62135-736-90) Available
Flurazepam Hydrochloride, Capsule, 30 mg (NDC 62135-737-30) Available
Flurazepam Hydrochloride, Capsule, 30 mg (NDC 62135-737-90) Available
Morphine Sulfate Injection
Piramal Critical Care Inc.
Analgesia/Addiction
2026-09-15
Currently in Shortage
First posted by the FDA
2017-10-31
Presentations affected
2
Manufacturer contact
800-414-1901
Mitigo, Injection, 200 mg/20 mL (NDC 66794-160-02) Available
Mitigo, Injection, 500 mg/20 mL (NDC 66794-162-02) Available
Penicillin G Benzathine Injection
Laboratorios Atral
Anti-Infective
2026-09-15
Currently in Shortage
First posted by the FDA
2023-04-26
Presentations affected
1
Manufacturer contact
Mark Cuban Cost Plus Drug Company: 682-428-8081
Lentocilin, Injection, 1200000 U/4 mL (NDC 84383-110-01) Available
More from the FDA
Rocuronium Bromide Injection
Piramal Critical Care Inc.
Anesthesia
2026-09-15
Currently in Shortage
First posted by the FDA
2023-02-15
Presentations affected
2
Manufacturer contact
800-414-1901
Rocuronium Bromide, Injection, 100 mg/10 mL (NDC 66794-229-41) Limited Availability Demand increase for the drug
Rocuronium Bromide, Injection, 50 mg/5 mL (NDC 66794-228-41) Available
Triamcinolone Hexacetonide Injection
Medexus
Rheumatology
2026-09-15
Currently in Shortage
First posted by the FDA
2021-05-04
Presentations affected
1
Manufacturer contact
1-855-336-3322 Option 9
Hexatrione, Injection, 40 mg/2 mL (NDC 59137-570-01) Available
More from the FDA
Atropine Sulfate Injection
Somerset Therapeutics, LLC
AnesthesiaNeurologyPediatric
2026-09-11
Currently in Shortage
First posted by the FDA
2012-01-01
Presentations affected
3
Manufacturer contact
732-554-1037
Atropine Sulfate, Injection, .4 mg/1 mL (NDC 70069-481-10) Available
Atropine Sulfate, Injection, .4 mg/1 mL (NDC 70069-631-25) Available
Atropine Sulfate, Injection, 1 mg/1 mL (NDC 70069-641-25) Available
Bupivacaine Hydrochloride Injection
Somerset Therapeutics, LLC
Anesthesia
2026-09-11
Currently in Shortage
First posted by the FDA
2018-02-20
Presentations affected
6
Manufacturer contact
732-554-1037
Bupivacaine Hydrochloride, Injection, 2.5 mg/1 mL (NDC 70069-752-01) Available
Bupivacaine Hydrochloride, Injection, 2.5 mg/1 mL (NDC 70069-752-10) Available
Bupivacaine Hydrochloride, Injection, 2.5 mg/1 mL (NDC 70069-752-25) Available
Bupivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 70069-753-01) Available
Bupivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 70069-753-10) Available
Bupivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 70069-753-25) Available
Cisatracurium Besylate Injection
Hospira, Inc., a Pfizer Company
Analgesia/Addiction
2026-09-11
To Be Discontinued
First posted by the FDA
2026-05-06
Presentations affected
3
Manufacturer contact
844-646-4398
Cisatracurium Besylate, Injection, 10 mg/5ml (2 mg/mL) Single Dose Vial (NDC 0409-1098-02)Supply expected to exhaust November 2026; Discontinuation of the manufacture of the drug
Cisatracurium Besylate, Injection, 20 mg/10 mL (2 mg/mL) Multidose Vial (NDC 0409-1208-01)Supply expected to exhaust late June 2026; Discontinuation of the manufacture of the drug
Cisatracurium Besylate, Injection, 200 mg/20ml (10 mg/mL) Single Dose Vial (NDC 0409-1103-01)Supply expected to exhaust late June 2026; Discontinuation of the manufacture of the drug
DELFLEX, Solution, 18.4 mg/100 mL; 4.25 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 46163-212-95)A business decision was made to discontinue manufacture of the drug.
Imipenem Anhydrous, Cilastatin, and Relebactam Anhydrous Injection
Merck Sharp & Dohme LLC
Anti-Infective
2026-09-09
To Be Discontinued
First posted by the FDA
2026-09-09
Presentations affected
1
Manufacturer contact
800-672-6372
RECARBRIO, Injection, 500 mg/100 mL; 500 mg/100 mL; 250 mg/100 mL (NDC 0006-3856-02)To be discontinued on or near late September 2026.
Ifosfamide Injection
SteriMax, Inc.
OncologyPediatric
2026-09-08
Currently in Shortage
First posted by the FDA
2026-06-12
Presentations affected
1
Manufacturer contact
877-373-4657
Ifosfamide, Injection, 1 g/1 (NDC 21586-211-02) Available To place an order, please contact GlobalRX at [email protected] or (919) 245-8418
More from the FDA
Clonazepam Tablet
Prinston Pharmaceutical, Inc.
NeurologyPediatricPsychiatry
2026-09-02
Currently in Shortage
First posted by the FDA
2023-03-10
Presentations affected
8
Manufacturer contact
For orders, Solco Healthcare 866-931-9829
Clonazepam, Tablet, .5 mg (NDC 43547-406-10) Available Marketed by Solco Healthcare
Clonazepam, Tablet, .5 mg (NDC 43547-406-11) Available Marketed by Solco Healthcare
Clonazepam, Tablet, .5 mg (NDC 43547-406-50) Available Marketed by Solco Healthcare
Clonazepam, Tablet, 1 mg (NDC 43547-407-10) Available Marketed by Solco Healthcare
Clonazepam, Tablet, 1 mg (NDC 43547-407-11) Available Marketed by Solco Healthcare
Clonazepam, Tablet, 1 mg (NDC 43547-407-50) Available Marketed by Solco Healthcare
Clonazepam, Tablet, 2 mg (NDC 43547-408-10) Available Marketed by Solco Healthcare
Clonazepam, Tablet, 2 mg (NDC 43547-408-50) Available Marketed by Solco Healthcare
RAVICTI, Oral Liquid, 1.1 g/1 mL (NDC 75987-050-06)Discontinuation in the manufacturing of the drug product
RAVICTI, Oral Liquid, 1.1 g/1 mL (NDC 75987-050-07)Discontinuation in the manufacturing of the drug product
Insulin Glargine-aglr Injection
Eli Lilly and Co.
Endocrinology/Metabolism
2026-09-01
To Be Discontinued
First posted by the FDA
2026-09-01
Presentations affected
1
Manufacturer contact
800-545-5979
Rezvoglar, Injection, 100 [iU]/1 mL (NDC 0002-8980-05)A business decision was made to discontinue manufacture of the drug. Distribution projected to end June 2027. If patients or prescribers have any questions, the Lilly Answers Center (1-800-545-5979) is available Monday through Friday from 9am to 8pm for assistance.
Insulin Lispro Injection
Eli Lilly and Co.
Endocrinology/Metabolism
2026-09-01
To Be Discontinued
First posted by the FDA
2025-10-24
Presentations affected
2
Manufacturer contact
800-545-5979
Insulin Lispro Junior KwikPen, Injection, 100 [iU]/1 mL (NDC 0002-7752-05)A business decision was made to discontinue manufacture of the drug. Distribution projected to end June 2027. If patients or prescribers have any questions, the Lilly Answers Center (1-800-545-5979) is available Monday through Friday from 9am to 8pm for assistance.
Humalog, Injection, U-100 Tempo Pen (NDC 0002-8213-05)A business decision was made to discontinue manufacture of the drug.
Insulin Lispro Protamine and Insulin Lispro Injection
Eli Lilly and Co.
Endocrinology/Metabolism
2026-09-01
To Be Discontinued
First posted by the FDA
2026-09-01
Presentations affected
1
Manufacturer contact
800-545-5979
Humalog Mix 75/25, Injection, 100 [iU]/1 mL (NDC 0002-8233-05)A business decision was made to discontinue manufacture of the drug. Distribution projected to end June 2027. If patients or prescribers have any questions, the Lilly Answers Center (1-800-545-5979) is available Monday through Friday from 9am to 8pm for assistance.
Medroxyprogesterone Acetate Tablet
Pfizer Inc.
Urology
2026-08-31
To Be Discontinued
First posted by the FDA
2026-08-31
Presentations affected
2
Manufacturer contact
800-533-4535
PROVERA, Tablet, 10 mg (NDC 0009-0051-01)Discontinuation of the manufacture of the drug; Withdrawal from sale expected September 2026.
PROVERA, Tablet, 2.5 mg (NDC 0009-0065-01)Discontinuation of the manufacture of the drug; Withdrawal from sale expected early October 2026.
Metoprolol Succinate Tablet, Extended Release
Teva Pharmaceuticals USA, Inc.
Cardiovascular
2026-08-31
To Be Discontinued
First posted by the FDA
2026-08-31
Presentations affected
7
Manufacturer contact
800-545-8800
Metoprolol Succinate, Tablet, Extended Release, 100 mg (NDC 45963-677-11)A business decision was made to discontinue manufacture of the drug.
Metoprolol Succinate, Tablet, Extended Release, 100 mg (NDC 45963-677-96)A business decision was made to discontinue manufacture of the drug.
Metoprolol Succinate, Tablet, Extended Release, 200 mg (NDC 45963-678-11)A business decision was made to discontinue manufacture of the drug.
Metoprolol Succinate, Tablet, Extended Release, 25 mg (NDC 45963-709-11)A business decision was made to discontinue manufacture of the drug.
Metoprolol Succinate, Tablet, Extended Release, 25 mg (NDC 45963-709-96)A business decision was made to discontinue manufacture of the drug.
Metoprolol Succinate, Tablet, Extended Release, 50 mg (NDC 45963-676-11)A business decision was made to discontinue manufacture of the drug.
Metoprolol Succinate, Tablet, Extended Release, 50 mg (NDC 45963-676-96)A business decision was made to discontinue manufacture of the drug.
Palovarotene Capsule
Ipsen Biopharmaceuticals, Inc.
Musculoskeletal
2026-08-31
To Be Discontinued
First posted by the FDA
2026-08-31
Presentations affected
1
Manufacturer contact
(855)-463-5127
SOHONOS, Capsule, 2.5 mg (NDC 15054-0025-1)Discontinuation of the manufacture of the drug
Cardioplegic Solution, Injection, Solution, 17.6 mg/100 mL; 325.3 mg/100 mL; 119.3 mg/100 mL; 643 mg/100 mL (NDC 65219-258-10)Discontinuation of the manufacture of the drug
Albuterol Sulfate Solution
Nephron Pharmaceuticals Corporation
PediatricPulmonary/Allergy
2026-08-27
Shortage Resolved
First posted by the FDA
2022-10-25
Presentations affected
1
Manufacturer contact
800-443-4313
Albuterol Sulfate, Solution, 2.5 mg/.5 mL (NDC 0487-9901-30)
Albuterol Sulfate Solution
Rising Pharma Holdings, Inc.
PediatricPulmonary/Allergy
2026-08-27
Shortage Resolved
First posted by the FDA
2022-10-25
Presentations affected
1
Manufacturer contact
201-961-9000
Albuterol Sulfate, Solution, 2.5 mg/.5 mL (NDC 64980-642-03)
Albuterol Sulfate Solution
Ritedose Pharmaceuticals, LLC
PediatricPulmonary/Allergy
2026-08-27
Shortage Resolved
First posted by the FDA
2022-10-25
Presentations affected
1
Manufacturer contact
803-806-3300
Albuterol Sulfate, Solution, 2.5 mg/.5 mL (NDC 76204-027-01)
Azacitidine Injection
Meitheal Pharmaceuticals, Inc.
Oncology
2026-08-27
Currently in Shortage
First posted by the FDA
2020-12-18
Presentations affected
1
Manufacturer contact
844-824-8426
Azacitidine, Injection, 100 mg/30 mL (NDC 71288-115-30) Available
Dexmedetomidine Hydrochloride Injection
Meitheal Pharmaceuticals, Inc.
Anesthesia
2026-08-27
Currently in Shortage
First posted by the FDA
2021-04-10
Presentations affected
1
Manufacturer contact
844-824-8426
Dexmedetomidine Hydrochloride, Injection, 100 ug/1 mL (NDC 71288-505-03) Available
Furosemide Injection
Meitheal Pharmaceuticals, Inc.
Cardiovascular
2026-08-27
Currently in Shortage
First posted by the FDA
2020-04-07
Presentations affected
3
Manufacturer contact
844-824-8426
Furosemide, Injection, 10 mg/1 mL (NDC 71288-203-05) Available Check wholesalers for inventory
Furosemide, Injection, 10 mg/1 mL (NDC 71288-203-11) Available Check wholesalers for inventory
Furosemide, Injection, 10 mg/mL, 2 mL (NDC 71288-205-03) Available Check wholesalers for inventory
Liraglutide Injection
Meitheal Pharmaceuticals, Inc.
Endocrinology/Metabolism
2026-08-27
Currently in Shortage
First posted by the FDA
2023-07-18
Presentations affected
2
Manufacturer contact
844-824-8426
Liraglutide, Injection, 6 mg/1 mL (NDC 71288-563-84) Available
Liraglutide, Injection, 6 mg/1 mL (NDC 71288-563-85) Available
Pegasys, Injection, 180 ug/.5 mL (NDC 82154-0451-4)
Pegasys, Injection, 180 ug/1 mL (NDC 82154-0449-1)
Rocuronium Bromide Injection
Meitheal Pharmaceuticals, Inc.
Anesthesia
2026-08-27
Currently in Shortage
First posted by the FDA
2023-02-15
Presentations affected
2
Manufacturer contact
844-824-8426
Rocuronium Bromide, Injection, 10 mg/1 mL (NDC 71288-700-06) Available
Rocuronium Bromide, Injection, 10 mg/1 mL (NDC 71288-718-11) Available
Liraglutide Injection
Novo Nordisk, Inc.
Endocrinology/Metabolism
2026-08-25
To Be Discontinued
First posted by the FDA
2026-08-25
Presentations affected
1
Manufacturer contact
833-493-4689
Saxenda, Injection, 6 mg/1 mL (NDC 0169-2800-15)Product will be available until discontinuation in January 2027; Discontinuation of the manufacture of the drug
Mesalamine Capsule, Extended Release
Mylan Pharmaceuticals Inc., a Viatris Company
Gastroenterology
2026-08-25
To Be Discontinued
First posted by the FDA
2026-08-25
Presentations affected
1
Manufacturer contact
800-796-9526
Mesalamine, Capsule, Extended Release, .375 g (NDC 0378-1375-78)Discontinuation of the manufacture of the drug
Disopyramide Phosphate Capsule, Extended Release
Pfizer Inc.
Cardiovascular
2026-08-24
To Be Discontinued
First posted by the FDA
2026-08-24
Presentations affected
2
Manufacturer contact
800-533-4535
Norpace CR, Capsule, Extended Release, 100 mg (NDC 0025-2732-31)Discontinuation of the manufacture of the drug
Norpace CR, Capsule, Extended Release, 150 mg (NDC 0025-2742-31)Discontinuation of the manufacture of the drug
DIANEAL Low Calcium with Dextrose, Intraperitoneal Injection, Solution, 18.3 mg/100 mL; 1.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0409-07)A business decision was made to discontinue manufacture of the drug.
DIANEAL Low Calcium with Dextrose, Intraperitoneal Injection, Solution, 18.3 mg/100 mL; 1.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0424-51)A business decision was made to discontinue manufacture of the drug.
DIANEAL Low Calcium with Dextrose, Intraperitoneal Injection, Solution, 18.3 mg/100 mL; 2.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0430-51)A business decision was made to discontinue manufacture of the drug.
DIANEAL Low Calcium with Dextrose, Intraperitoneal Injection, Solution, 18.3 mg/100 mL; 2.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0457-05)A business decision was made to discontinue manufacture of the drug.
DIANEAL Low Calcium with Dextrose, Intraperitoneal Injection, Solution, 18.3 mg/100 mL; 4.25 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0433-51)A business decision was made to discontinue manufacture of the drug.
DIANEAL Low Calcium with Dextrose, Intraperitoneal Injection, Solution, 18.3 mg/100 mL; 4.25 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0459-05)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 1.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0411-06)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 1.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0411-07)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 1.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0426-52)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 1.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0426-53)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 2.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0413-06)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 2.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0413-07)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 2.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0427-52)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 2.5 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0427-53)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 4.25 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0415-06)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 4.25 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0415-07)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 4.25 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0429-52)A business decision was made to discontinue manufacture of the drug.
DIANEAL PD-2 with Dextrose, Intraperitoneal Injection, Solution, 25.7 mg/100 mL; 4.25 g/100 mL; 5.08 mg/100 mL; 538 mg/100 mL; 448 mg/100 mL (NDC 0941-0429-53)A business decision was made to discontinue manufacture of the drug.
Triamcinolone Acetonide Injection
Harrow Eye, LLC
Ophthalmology
2026-07-31
Shortage Resolved
First posted by the FDA
2021-09-27
Presentations affected
1
Manufacturer contact
(615) 733-4734
Triesence, Injection, 40 mg/1 mL (NDC 82667-800-01)
Lidocaine Hydrochloride, Injection, 10 mg/1 mL (NDC 73293-0001-2) Unavailable Demand increase for the drug
Fluticasone Propionate and Salmeterol Xinafoate Aerosol, Metered
GlaxoSmithKline
Pulmonary/Allergy
2026-07-27
To Be Discontinued
First posted by the FDA
2026-07-27
Presentations affected
3
Manufacturer contact
888-825-5249
Advair HFA, Aerosol, Metered, 115 ug; 21 ug (NDC 0173-0716-22)The anticipated date that GSK will cease distribution of the presentation is approximately December 31, 2026. The 120 dose presentation of this product will still be available.
Advair HFA, Aerosol, Metered, 230 ug; 21 ug (NDC 0173-0717-22)The anticipated date that GSK will cease distribution of the presentation is approximately December 31, 2026. The 120 dose presentation of this product will still be available.
Advair HFA, Aerosol, Metered, 45 ug; 21 ug (NDC 0173-0715-22)The anticipated date that GSK will cease distribution of the presentation is approximately December 31, 2026. The 120 dose presentation of this product will still be available.
Lopinavir and Ritonavir Oral Solution
AbbVie Inc.
Antiviral
2026-07-24
To Be Discontinued
First posted by the FDA
2026-07-24
Presentations affected
1
Manufacturer contact
800-633-9110
Kaletra, Oral Solution, 80 mg/1 mL; 20 mg/1 mL (NDC 0074-3956-46)Discontinuation of the manufacture of the drug
Lopinavir and Ritonavir Tablet
AbbVie Inc.
Antiviral
2026-07-24
To Be Discontinued
First posted by the FDA
2026-07-24
Presentations affected
4
Manufacturer contact
800-633-9110
Kaletra, Tablet, 100 mg; 25 mg (NDC 0074-0522-60)Discontinuation of the manufacture of the drug
Kaletra, Tablet, 100 mg; 25 mg (NDC 0074-3008-60)Discontinuation of the manufacture of the drug
Kaletra, Tablet, 200 mg; 50 mg (NDC 0074-4014-12)Discontinuation of the manufacture of the drug
Kaletra, Tablet, 200 mg; 50 mg (NDC 0074-6799-22)Discontinuation of the manufacture of the drug
Ritonavir Oral Powder
AbbVie Inc.
Antiviral
2026-07-24
To Be Discontinued
First posted by the FDA
2026-07-24
Presentations affected
1
Manufacturer contact
800-633-9110
Norvir, Oral Powder, 100 mg (NDC 0074-3399-30)Discontinuation of the manufacture of the drug
Ritonavir Tablet
AbbVie Inc.
Antiviral
2026-07-24
To Be Discontinued
First posted by the FDA
2026-07-24
Presentations affected
1
Manufacturer contact
800-633-9110
Norvir, Tablet, 100 mg (NDC 0074-2340-30)Discontinuation of the manufacture of the drug
Aspirin Suppository
Padagis US LLC
Analgesia/AddictionCardiovascular
2026-07-23
To Be Discontinued
First posted by the FDA
2026-07-23
Presentations affected
1
Manufacturer contact
(800) 775-2054
Aspirin, Suppository, 300 mg (NDC 0574-7034-12)Discontinuation of the manufacture of the drug
Belladonna and Opium Suppository
Padagis US LLC
Analgesia/Addiction
2026-07-23
To Be Discontinued
First posted by the FDA
2026-07-23
Presentations affected
4
Manufacturer contact
(800) 775-2054
Belladonna and Opium, Suppository, 16.2 mg; 30 mg (NDC 0574-7045-04)Discontinuation of the manufacture of the drug
Belladonna and Opium, Suppository, 16.2 mg; 30 mg (NDC 0574-7045-12)Discontinuation of the manufacture of the drug
Belladonna and Opium, Suppository, 16.2 mg; 60 mg (NDC 0574-7040-04)Discontinuation of the manufacture of the drug
Belladonna and Opium, Suppository, 16.2 mg; 60 mg (NDC 0574-7040-12)Discontinuation of the manufacture of the drug
Bendamustine Hydrochloride Injection, Solution
Cephalon, LLC (a wholly owned subsidiary of Teva Pharmaceutical Industries, Ltd.)
Oncology
2026-07-23
To Be Discontinued
First posted by the FDA
2026-07-23
Presentations affected
1
Manufacturer contact
(610) 344-0200
Treanda, Injection, Solution, 25 mg/5 mL, 1 vial, Single-Dose in 1 carton (NDC 63459-390-08)A business decision has been made to discontinue manufacture of the drug.
Hydrocortisone Acetate Suppository
Padagis US LLC
Analgesia/AddictionOther
2026-07-23
To Be Discontinued
First posted by the FDA
2026-07-23
Presentations affected
2
Manufacturer contact
(800) 775-2054
Hydrocortisone Acetate, Suppository, 25 mg (NDC 0574-7090-12)Discontinuation of the manufacture of the drug
Hydrocortisone Acetate, Suppository, 30 mg (NDC 0574-7093-12)Discontinuation of the manufacture of the drug
Hydromorphone Hydrochloride Suppository
Padagis US LLC
Analgesia/Addiction
2026-07-23
To Be Discontinued
First posted by the FDA
2026-07-23
Presentations affected
1
Manufacturer contact
(800) 775-2054
Hydromorphone Hydrochloride, Suppository, 3 mg (NDC 0574-7224-06)Discontinuation of the manufacture of the drug
Morphine Sulfate Suppository
Padagis US LLC
Analgesia/Addiction
2026-07-23
To Be Discontinued
First posted by the FDA
2026-07-23
Presentations affected
4
Manufacturer contact
(800) 775-2054
Morphine Sulfate, Suppository, 10 mg (NDC 0574-7112-12)Discontinuation of the manufacture of the drug
Morphine Sulfate, Suppository, 20 mg (NDC 0574-7114-12)Discontinuation of the manufacture of the drug
Morphine Sulfate, Suppository, 30 mg (NDC 0574-7116-12)Discontinuation of the manufacture of the drug
Morphine Sulfate, Suppository, 5 mg (NDC 0574-7110-12)Discontinuation of the manufacture of the drug
Podophyllum Resin Topical Tincture
Padagis US LLC
Dermatology
2026-07-23
To Be Discontinued
First posted by the FDA
2026-07-23
Presentations affected
1
Manufacturer contact
(800) 775-2054
Podocon 25, Topical Tincture, 1 mg/4 mL (NDC 0574-0601-15)Discontinuation of the manufacture of the drug
Succinylcholine Chloride Injection
Fresenius Kabi USA, LLC
Anesthesia
2026-07-23
To Be Discontinued
First posted by the FDA
2026-07-23
Presentations affected
1
Manufacturer contact
888-386-1300
Succinylcholine Chloride, Injection, 20 mg/1 mL (NDC 63323-943-10)Discontinuation of the manufacture of the drug
Bupivacaine Hydrochloride, Injection, 2.5 mg/1 mL (NDC 31722-275-32) Available
Bupivacaine Hydrochloride, Injection, 2.5 mg/1 mL (NDC 31722-275-34) Available
Bupivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 31722-276-32) Available
Bupivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 31722-276-34) Available
Bupivacaine Hydrochloride, Injection, 7.5 mg/1 mL (NDC 31722-277-32) Available
Bupivacaine Hydrochloride, Injection, 7.5 mg/1 mL (NDC 31722-277-34) Available
Tobramycin Sulfate Injection
Hospira, Inc., a Pfizer Company
Anti-Infective
2026-07-17
To Be Discontinued
First posted by the FDA
2026-07-17
Presentations affected
1
Manufacturer contact
844-646-4398
Tobramycin Sulfate, Injection, 80 mg/2 mL (40 mg/mL); 2 mL Multiple Dose Glass Fliptop Vial (NDC 0409-3578-01)Discontinuation of the manufacture of the drug
Travoprost Ophthalmic Solution
Mylan Pharmaceuticals Inc., a Viatris Company
Ophthalmology
2026-07-07
To Be Discontinued
First posted by the FDA
2026-07-07
Presentations affected
2
Manufacturer contact
877-446-3679
Travoprost, Ophthalmic Solution, 0.004%, 2.5 mL (NDC 0378-9651-32)Discontinuation of the manufacture of the drug
Travoprost, Ophthalmic Solution, 0.004%, 5 mL (NDC 0378-9651-50)Discontinuation of the manufacture of the drug
Daptomycin, Injection, 500 mg/10 mL (NDC 0143-9378-01)Discontinuation of the manufacture of the drug; Marketed by Hikma Pharmaceuticals USA, Inc.
Daptomycin, Injection, 500 mg/10 mL (NDC 57884-3151-1)Discontinuation of the manufacture of the drug
Gadobutrol Injection
Jiangsu Hengrui Pharmaceuticals Co., Ltd.
Medical Imaging
2026-06-30
To Be Discontinued
First posted by the FDA
2026-06-30
Presentations affected
4
Manufacturer contact
888-386-1300
Gadobutrol, Injection, 604.72 mg/mL (NDC 65219-281-02)Discontinuance of single dose vials, the other two Imaging Bulk Package(IBP) strengths are to remain in supply: the IBP strengths (18.1416 g/30 mL and 39.3068 g/65 mL); Marketed by Fresenius Kabi, USA
Gadobutrol, Injection, 604.72 mg/mL (NDC 65219-281-07)Discontinuance of single dose vials, the other two Imaging Bulk Package(IBP) strengths are to remain in supply: the IBP strengths (18.1416 g/30 mL and 39.3068 g/65 mL); Marketed by Fresenius Kabi, USA
Gadobutrol, Injection, 604.72 mg/mL (NDC 65219-281-10)Discontinuance of single dose vials, the other two Imaging Bulk Package(IBP) strengths are to remain in supply: the IBP strengths (18.1416 g/30 mL and 39.3068 g/65 mL); Marketed by Fresenius Kabi, USA
Gadobutrol, Injection, 604.72 mg/mL (NDC 65219-281-15)Discontinuance of single dose vials, the other two Imaging Bulk Package(IBP) strengths are to remain in supply: the IBP strengths (18.1416 g/30 mL and 39.3068 g/65 mL); Marketed by Fresenius Kabi, USA
Gadoterate Meglumine Injection
Jiangsu Hengrui Pharmaceuticals Co., Ltd.
Medical Imaging
2026-06-30
To Be Discontinued
First posted by the FDA
2026-06-30
Presentations affected
4
Manufacturer contact
888-386-1800
Gadoterate Meglumine, Injection, 376.9 mg/1 mL (NDC 65219-080-05)Marketed by Fresenius Kabi, USA; Discontinuation of the manufacture of the drug
Gadoterate Meglumine, Injection, 376.9 mg/1 mL (NDC 65219-082-10)Marketed by Fresenius Kabi, USA; Discontinuation of the manufacture of the drug
Gadoterate Meglumine, Injection, 376.9 mg/1 mL (NDC 65219-084-15)Marketed by Fresenius Kabi, USA; Discontinuation of the manufacture of the drug
Gadoterate Meglumine, Injection, 376.9 mg/1 mL (NDC 65219-086-20)Marketed by Fresenius Kabi, USA; Discontinuation of the manufacture of the drug
Lisdexamfetamine Dimesylate Capsule
Solco Healthcare US, LLC
Psychiatry
2026-06-29
Currently in Shortage
First posted by the FDA
2023-07-14
Presentations affected
7
Manufacturer contact
866-931-9829
Lisdexamfetamine Dimesylate, Capsule, 10 mg (NDC 43547-602-10) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 20 mg (NDC 43547-603-10) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 30 mg (NDC 43547-604-10) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 40 mg (NDC 43547-605-10) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 50 mg (NDC 43547-606-10) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 60 mg (NDC 43547-607-10) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 70 mg (NDC 43547-608-10) Limited Availability Shortage of an active ingredient
Oxaliplatin Injection
Jiangsu Hengrui Pharmaceuticals Co., Ltd.
Oncology
2026-06-29
To Be Discontinued
First posted by the FDA
2026-06-29
Presentations affected
2
Manufacturer contact
Sagent Pharmaceuticals: 866-625-1618
Oxaliplatin, Injection, 5 mg/1 mL (NDC 25021-233-10)Marketed by Sagent Pharmaceuticals; Discontinuation of the manufacture of the drug
Oxaliplatin, Injection, 5 mg/1 mL (NDC 25021-233-20)Marketed by Sagent Pharmaceuticals; Discontinuation of the manufacture of the drug
Quinapril Hydrochloride Tablet
Solco Healthcare US, LLC
Cardiovascular
2026-06-29
Currently in Shortage
First posted by the FDA
2023-01-19
Presentations affected
4
Manufacturer contact
866-931-9829
Quinapril Hydrochloride, Tablet, 10 mg (NDC 43547-411-09) Unavailable Shortage of an active ingredient
Quinapril Hydrochloride, Tablet, 20 mg (NDC 43547-412-09) Unavailable Shortage of an active ingredient
Quinapril Hydrochloride, Tablet, 40 mg (NDC 43547-413-09) Unavailable Shortage of an active ingredient
Quinapril Hydrochloride, Tablet, 5 mg (NDC 43547-410-09) Unavailable Shortage of an active ingredient
Lisdexamfetamine Dimesylate Capsule
Rhodes Pharmaceuticals L.P.
Psychiatry
2026-06-24
Currently in Shortage
First posted by the FDA
2023-07-14
Presentations affected
7
Manufacturer contact
888-827-0616
Lisdexamfetamine Dimesylate, Capsule, 10 mg (NDC 42858-161-01) Available
Lisdexamfetamine Dimesylate, Capsule, 20 mg (NDC 42858-162-01) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 30 mg (NDC 42858-163-01) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 40 mg (NDC 42858-164-01) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 50 mg (NDC 42858-165-01) Limited Availability Shortage of an active ingredient
Lisdexamfetamine Dimesylate, Capsule, 60 mg (NDC 42858-166-01) Available
Lisdexamfetamine Dimesylate, Capsule, 70 mg (NDC 42858-167-01) Limited Availability Shortage of an active ingredient
Emtricitabine Capsule
Gilead Sciences, Inc.
Anti-Infective
2026-06-17
To Be Discontinued
First posted by the FDA
2026-06-17
Presentations affected
1
Manufacturer contact
800-445-3235
Emtriva, Capsule, 200 mg (NDC 61958-0601-1)Product expected to be available until March 2027
Emtricitabine Oral Solution
Gilead Sciences, Inc.
Anti-Infective
2026-06-17
To Be Discontinued
First posted by the FDA
2026-06-17
Presentations affected
1
Manufacturer contact
800-445-3235
Emtriva, Oral Solution, 10 mg/1 mL (NDC 61958-0602-1)Product expected to be available until March 2027
Etomidate Injection
Caplin Steriles, Ltd.
Anesthesia
2026-06-16
Currently in Shortage
First posted by the FDA
2022-10-05
Presentations affected
4
Manufacturer contact
908-803-2586
Etomidate, Injection, 2 mg/mL (NDC 72485-508-10) Available Check wholesalers for inventory; Marketed by Armas Pharmaceuticals, Inc. 908-803-2586
Etomidate, Injection, 2 mg/mL (NDC 72485-509-10) Available Check wholesalers for inventory; Marketed by Armas Pharmaceuticals, Inc. 908-803-2586
Etomidate, Injection, 2mg/1 mL (NDC 65219-445-10) Available Check wholesalers for inventory; Marketed by Fresenius Kabi
Etomidate, Injection, 2mg/mL (NDC 65219-447-20) Available Check wholesalers for inventory; Marketed by Fresenius Kabi
Cefotaxime Sodium Powder, for Solution
SteriMax, Inc.
Anti-InfectivePediatric
2026-06-15
Currently in Shortage
First posted by the FDA
2015-02-17
Presentations affected
2
Manufacturer contact
800-881-3550
Cefotaxime Sodium, Powder, for Solution, 1 g (NDC 21586-011-02) Available
More from the FDA
Cefotaxime Sodium, Powder, for Solution, 2 g (NDC 21586-012-02) Available
More from the FDA
Donepezil Hydrochloride; Memantine Hydrochloride, Capsule, Extended Release, 10 mg; 14 mg (NDC 69238-1248-3)Discontinuation of the manufacture of the drug
Donepezil Hydrochloride; Memantine Hydrochloride, Capsule, Extended Release, 10 mg; 28 mg (NDC 69238-1247-3)Discontinuation of the manufacture of the drug
Lorlatinib Tablet
Pfizer Inc.
Oncology
2026-06-15
To Be Discontinued
First posted by the FDA
2026-06-15
Presentations affected
1
Manufacturer contact
800-533-4535
Lorbrena, Tablet, 25 mg; 120 tablets bottle with a child-resistant closure (NDC 0069-0227-03)Supply expected to exhaust 6/30/2026; NDC 0069-0227-01 25 mg; 30 tablets bottle with a child-resistant closure will continue to be manufactured; Discontinuation of the manufacture of this presentation
Ropivacaine Hydrochloride Injection
Caplin Steriles, Ltd.
Anesthesia
2026-06-10
Currently in Shortage
First posted by the FDA
2020-12-22
Presentations affected
4
Manufacturer contact
888-229-0001
Ropivacaine Hydrochloride, Injection, 10 mg/1 mL (NDC 43066-027-10) Available Check wholesalers for inventory; Marketed by Baxter
Ropivacaine Hydrochloride, Injection, 2 mg/1 mL (NDC 43066-015-10) Limited Availability Other
Ropivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 43066-019-10) Available Check wholesalers for inventory; Marketed by Baxter
Ropivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 43066-023-10) Limited Availability Other
Azacitidine Injection
Armas Pharmaceuticals Inc
Oncology
2026-06-08
Currently in Shortage
First posted by the FDA
2020-12-18
Presentations affected
1
Manufacturer contact
732-637-1971
Azacitidine, Injection, 100 mg (NDC 72485-201-01) Limited Availability Other
Dacomitinib Tablet
Pfizer Inc.
Oncology
2026-06-08
To Be Discontinued
First posted by the FDA
2026-06-08
Presentations affected
3
Manufacturer contact
800-533-4535
Vizimpro, Tablet, 15 mg (NDC 0069-0197-30)Discontinuation of the manufacture of the drug
Vizimpro, Tablet, 30 mg (NDC 0069-1198-30)Discontinuation of the manufacture of the drug
Vizimpro, Tablet, 45 mg (NDC 0069-2299-30)Discontinuation of the manufacture of the drug
Leflunomide Tablet
Sanofi-Aventis U.S. LLC
Rheumatology
2026-06-08
To Be Discontinued
First posted by the FDA
2026-06-08
Presentations affected
5
Manufacturer contact
800-981-2491
Arava, Tablet, 10 mg (NDC 0088-2160-30)Discontinuation of the manufacture of the drug
Arava, Tablet, 100 mg (NDC 0088-2162-33)Discontinuation of the manufacture of the drug
Arava, Tablet, 20 mg (NDC 0088-2161-30)Discontinuation of the manufacture of the drug
Leflunomide, Tablet, 10 mg (NDC 0955-1735-30)Discontinuation of the manufacture of the drug
Leflunomide, Tablet, 20 mg (NDC 0955-1737-30)Discontinuation of the manufacture of the drug
Dexmedetomidine Hydrochloride Injection
Slayback Pharma
Anesthesia
2026-06-05
To Be Discontinued
First posted by the FDA
2026-06-05
Presentations affected
2
Manufacturer contact
800-461-7449
Dexmedetomidine Hydrochloride, Injection, 4 ug/1 mL (NDC 71225-126-05)Discontinuation of the manufacture of the drug
Dexmedetomidine Hydrochloride, Injection, 4 ug/1 mL (NDC 71225-126-06)Discontinuation of the manufacture of the drug
Semaglutide Tablet
Novo Nordisk, Inc.
Endocrinology/Metabolism
2026-06-04
To Be Discontinued
First posted by the FDA
2026-06-04
Presentations affected
3
Manufacturer contact
833-493-4689
Rybelsus, Tablet, 14 mg (NDC 0169-4314-30)Discontinuation of the manufacture of the drug. These products will be replaced by Ozempic (semaglutide) tablets.
Rybelsus, Tablet, 3 mg (NDC 0169-4303-30)Discontinuation of the manufacture of the drug. These products will be replaced by Ozempic (semaglutide) tablets.
Rybelsus, Tablet, 7 mg (NDC 0169-4307-30)Discontinuation of the manufacture of the drug. These products will be replaced by Ozempic (semaglutide) tablets.
Bacitracin Ophthalmic Ointment
Padagis US LLC
Anti-InfectiveOphthalmology
2026-06-01
Currently in Shortage
First posted by the FDA
2025-03-03
Presentations affected
1
Manufacturer contact
866-634-9120
Bacitracin, Ophthalmic Ointment, 3.5 g (NDC 0574-4022-35) Unavailable Discontinuation of the manufacture of the drug
Carboplatin Injection
Teyro Labs
Oncology
2026-06-01
To Be Discontinued
First posted by the FDA
2026-06-01
Presentations affected
4
Manufacturer contact
Apotex Inc.: 800-706-5575
Carboplatin, Injection, 150 mg/15 mL (10 mg/mL) Multiple Dose Vial (NDC 60505-6282-3)Wholesaler & Distributor through Marketing partner (Apotex Inc.); Discontinuation of the manufacture of the drug
Carboplatin, Injection, 450 mg/45 mL (10 mg/mL) Multiple Dose Vial (NDC 60505-6282-6)Wholesaler & Distributor through Marketing partner (Apotex Inc.); Discontinuation of the manufacture of the drug
Carboplatin, Injection, 50 mg/5 mL (10 mg/mL) Multiple Dose Vial (NDC 60505-6282-1)Wholesaler & Distributor through Marketing partner (Apotex Inc.); Discontinuation of the manufacture of the drug
Carboplatin, Injection, 600 mg/60 mL (10 mg/mL) Multiple Dose Vial (NDC 60505-6282-7)Wholesaler & Distributor through Marketing partner (Apotex Inc.); Discontinuation of the manufacture of the drug
Clindamycin Phosphate Injection
Pfizer Inc.
Anti-Infective
2026-06-01
To Be Discontinued
First posted by the FDA
2026-06-01
Presentations affected
6
Manufacturer contact
844-646-4398
Cleocin Phosphate, Injection, 300 mg/2 mL (150 mg/mL); 2 mL Vial (NDC 0009-0870-26)Discontinuation of the manufacture of the drug
Cleocin Phosphate, Injection, 300 mg/2 mL (150 mg/mL); 2 mL Vial NovaPlus (NDC 0009-3051-02)Discontinuation of the manufacture of the drug
Cleocin Phosphate, Injection, 600 mg/4 mL (150 mg/mL); 4 mL Vial (NDC 0009-0775-26)Discontinuation of the manufacture of the drug
Cleocin Phosphate, Injection, 600 mg/4 mL (150 mg/mL); 4 mL Vial NovaPlus (NDC 0009-4073-04)Discontinuation of the manufacture of the drug
Cleocin Phosphate, Injection, 900 mg/6 mL (150 mg/mL); 6 mL Vial (NDC 0009-0902-18)Discontinuation of the manufacture of the drug
Cleocin Phosphate, Injection, 900 mg/6 mL (150 mg/mL); 6 mL Vial NovaPlus (NDC 0009-5095-06)Discontinuation of the manufacture of the drug
Clonazepam, Tablet, .5 mg (NDC 72888-152-00) Available Marketed by Advagen Pharma Ltd.
Clonazepam, Tablet, .5 mg (NDC 72888-152-01) Available Marketed by Advagen Pharma Ltd.
Clonazepam, Tablet, .5 mg (NDC 72888-152-05) Available Marketed by Advagen Pharma Ltd.
Clonazepam, Tablet, .5 mg (NDC 72888-152-30) Available Marketed by Advagen Pharma Ltd.
Clonazepam, Tablet, 1 mg (NDC 72888-153-00) Available Marketed by Advagen Pharma Ltd.
Clonazepam, Tablet, 1 mg (NDC 72888-153-01) Available Marketed by Advagen Pharma Ltd.
Clonazepam, Tablet, 1 mg (NDC 72888-153-05) Available Marketed by Advagen Pharma Ltd.
Clonazepam, Tablet, 1 mg (NDC 72888-153-30) Available Marketed by Advagen Pharma Ltd.
Clonazepam, Tablet, 2 mg (NDC 72888-154-01) Available Marketed by Advagen Pharma Ltd.
Clonazepam, Tablet, 2 mg (NDC 72888-154-05) Available Marketed by Advagen Pharma Ltd.
Clonazepam, Tablet, 2 mg (NDC 72888-154-30) Available Marketed by Advagen Pharma Ltd.
Dehydrated Alcohol Injection, Solution
Accord Healthcare Inc.
Cardiovascular
2026-05-27
To Be Discontinued
First posted by the FDA
2026-05-27
Presentations affected
1
Manufacturer contact
866-941-7875
Dehydrated Alcohol, Injection, Solution, 1 mL/1 mL (10 pack) (NDC 16729-710-45)Accord is transitioning to the 5-pack configuration (NDC 16729-710-53).
Alteplase Injection
Genentech, Inc
CardiovascularHematologyNeurology
2026-05-21
To Be Discontinued
First posted by the FDA
2026-05-21
Presentations affected
1
Manufacturer contact
800-551-2231
Activase, Injection, 1 KIT in 1 CARTON (50242-085-27) * 100 mL in 1 VIAL, SINGLE-USE * 100 mL in 1 VIAL, SINGLE USE (NDC 50242-085-27)Discontinuation of the 100mg vial configuration
Iron Sucrose Injection
Mylan Institutional, a Viatris Company
Hematology
2026-05-21
To Be Discontinued
First posted by the FDA
2026-05-21
Presentations affected
1
Manufacturer contact
800-796-9526
Iron Sucrose, Injection, 50 mg/2.5 mL (NDC 67457-957-99)A business decision has been made to discontinue of 2.5mL presentation only. Continuity of supply is forecasted across all other presentations of Iron Sucrose: 67457-639-10 Iron Sucrose 20mg/mL 10mL SDV 5PK 67457-638-10 Iron Sucrose 20mg/mL 5mL SDV 10PK 67457-638-25 Iron Sucrose 20mg/mL 5mL SDV 25PK.
Activated Charcoal Oral Suspension
Padagis US LLC
Other
2026-05-15
To Be Discontinued
First posted by the FDA
2026-05-15
Presentations affected
5
Manufacturer contact
866-634-9120
Actidose Aqua, Oral Suspension, 208 mg/1 mL (NDC 0574-0521-25)Discontinuation of the manufacture of the drug
Actidose Aqua, Oral Suspension, 208 mg/1 mL (NDC 0574-0521-74)Discontinuation of the manufacture of the drug
Actidose Aqua, Oral Suspension, 208 mg/1 mL (NDC 0574-0521-76)Discontinuation of the manufacture of the drug
Actidose, Oral Suspension, 208 mg/1 mL (NDC 0574-0520-74)Discontinuation of the manufacture of the drug
Actidose, Oral Suspension, 208 mg/1 mL (NDC 0574-0520-76)Discontinuation of the manufacture of the drug
Ketorolac Tromethamine Injection
Alembic Pharmaceuticals
Analgesia/Addiction
2026-05-15
Currently in Shortage
First posted by the FDA
2018-03-23
Presentations affected
3
Manufacturer contact
908-393-9604
Ketorolac Tromethamine, Injection, 15 mg/1 mL (NDC 62332-599-25) Available
Ketorolac Tromethamine, Injection, 30 mg/1 mL (NDC 62332-600-25) Available
Ketorolac Tromethamine, Injection, 60 mg/2 mL (NDC 62332-601-25) Available
Liraglutide Injection
Teva Pharmaceuticals USA, Inc.
Endocrinology/Metabolism
2026-05-14
To Be Discontinued
First posted by the FDA
2026-05-14
Presentations affected
1
Manufacturer contact
888-838-2872
Liraglutide, Injection, 6 mg/1 mL (NDC 0480-7250-46)Discontinuation of the manufacture of the drug
Sulconazole Nitrate Solution
Journey Medical Corporation
Dermatology
2026-05-08
To Be Discontinued
First posted by the FDA
2026-05-08
Presentations affected
3
Manufacturer contact
480-434-6670
Exelderm, Solution, 1.0% 30 mL (NDC 69489-721-30)Discontinuation of the manufacture of the drug
Exelderm, Solution, 1.0% 5 mL (NDC 69489-721-05)Discontinuation of the manufacture of the drug
Sulconazole Nitrate, Solution, 30 mL (NDC 72143-321-30)Discontinuation of the manufacture of the drug. Manufactured for JG Pharma
Icatibant Acetate Injection
Fresenius Kabi USA, LLC
Hematology
2026-05-07
To Be Discontinued
First posted by the FDA
2026-05-07
Presentations affected
2
Manufacturer contact
847-550-2300
Icatibant Acetate, Injection, 10 mg/1 mL (NDC 63323-574-86)Discontinuation of the manufacturer of the drug
Icatibant Acetate, Injection, 10 mg/1 mL (NDC 63323-574-93)Discontinuation of the manufacturer of the drug
Bupivacaine Hydrochloride Injection
Kindos Pharmaceuticals Co. Ltd.
Anesthesia
2026-05-05
To Be Discontinued
First posted by the FDA
2026-05-05
Presentations affected
5
Manufacturer contact
844-824-8426
Bupivacaine Hydrochloride, Injection, 2.5 mg/1 mL (NDC 71288-722-32)Discontinuation of the manufacture of the drug
Bupivacaine Hydrochloride, Injection, 2.5 mg/1 mL (NDC 71288-723-52)Discontinuation of the manufacture of the drug
Bupivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 71288-725-32)Discontinuation of the manufacture of the drug
Bupivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 71288-726-52)Discontinuation of the manufacture of the drug
Bupivacaine Hydrochloride, Injection, 7.5 mg/1 mL (NDC 71288-728-32)Discontinuation of the manufacture of the drug
Bupivacaine Hydrochloride Injection
Kindos Pharmaceuticals Co. Ltd.
Anesthesia
2026-05-05
Currently in Shortage
First posted by the FDA
2018-02-20
Presentations affected
5
Manufacturer contact
844-824-8426
Bupivacaine Hydrochloride, Injection, 2.5 mg/1 mL (NDC 71288-722-32) Limited Availability Discontinuation of the manufacture of the drug
More from the FDA
Bupivacaine Hydrochloride, Injection, 2.5 mg/1 mL (NDC 71288-723-52) Limited Availability Discontinuation of the manufacture of the drug
More from the FDA
Bupivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 71288-725-32) Limited Availability Discontinuation of the manufacture of the drug
More from the FDA
Bupivacaine Hydrochloride, Injection, 5 mg/1 mL (NDC 71288-726-52) Limited Availability Discontinuation of the manufacture of the drug
More from the FDA
Bupivacaine Hydrochloride, Injection, 7.5 mg/1 mL (NDC 71288-728-32) Limited Availability Discontinuation of the manufacture of the drug
More from the FDA
Desmopressin Acetate Spray
Ferring
Hematology
2026-05-01
Currently in Shortage
First posted by the FDA
2021-03-12
Presentations affected
3
Manufacturer contact
888-337-7464
Ddavp, Spray, .1 ug/1 mL (NDC 55566-2500-0) Unavailable Requirements related to complying with good manufacturing practices
Desmopressin Acetate, Spray, 10 ug/.1 mL (NDC 69918-501-05) Unavailable Requirements related to complying with good manufacturing practices
Stimate, Spray, 1.5 mg/1 mL (NDC 0053-6871-00) Unavailable Requirements related to complying with good manufacturing practices
Lamotrigine Tablet, Extended Release
Par Health, Inc.
Neurology
2026-04-29
To Be Discontinued
First posted by the FDA
2026-04-29
Presentations affected
6
Manufacturer contact
800-828-9393
Lamotrigine, Tablet, Extended Release, 100 mg (NDC 49884-563-11)Discontinuation of the manufacture of the drug
Lamotrigine, Tablet, Extended Release, 200 mg (NDC 49884-564-11)Discontinuation of the manufacture of the drug
Lamotrigine, Tablet, Extended Release, 25 mg (NDC 49884-561-11)Discontinuation of the manufacture of the drug
Lamotrigine, Tablet, Extended Release, 250 mg (NDC 49884-604-11)Discontinuation of the manufacture of the drug
Lamotrigine, Tablet, Extended Release, 300 mg (NDC 49884-605-11)Discontinuation of the manufacture of the drug
Lamotrigine, Tablet, Extended Release, 50 mg (NDC 49884-562-11)Discontinuation of the manufacture of the drug
Crinecerfont Capsule
Neurocrine Biosciences, Inc.
Endocrinology/Metabolism
2026-04-28
To Be Discontinued
First posted by the FDA
2026-04-28
Presentations affected
1
Manufacturer contact
858-617-7600
Crenessity, Capsule, 25 mg (NDC 70370-5025-1)Neurocrine is discontinuing only the 25 mg soft gel capsule dose strength (NDC 70370-5025-01). The 50mg and 100mg soft gel capsule dose strength (NDC 70370-5050-1 and 70370-5100-1), and 50 mg/mL oral solution will continue to be marketed (NDC 70370-5250-1).
Etravirine Tablet
Janssen Research and Development
Antiviral
2026-04-28
To Be Discontinued
First posted by the FDA
2026-04-28
Presentations affected
2
Manufacturer contact
800-526-7736
Etravirine, Tablet, 100 mg (NDC 10147-0570-1)Discontinuation of the manufacture of the drug
Intelence, Tablet, 100 mg (NDC 59676-570-01)Discontinuation of the manufacture of the drug
Furosemide Injection
Gland Pharma Limited
Cardiovascular
2026-04-28
To Be Discontinued
First posted by the FDA
2026-04-28
Presentations affected
3
Manufacturer contact
Sagent Pharmaceuticals: 866-625-1618
Furosemide, Injection, 10 mg/1 mL (NDC 25021-311-02)Distributed by Sagent Pharmaceuticals; Discontinuation of the manufacture of the drug
Furosemide, Injection, 10 mg/1 mL (NDC 25021-311-04)Distributed by Sagent Pharmaceuticals; Discontinuation of the manufacture of the drug
Furosemide, Injection, 10 mg/1 mL (NDC 25021-311-10)Distributed by Sagent Pharmaceuticals; Discontinuation of the manufacture of the drug
Palbociclib Capsule
Pfizer Inc.
Oncology
2026-04-22
To Be Discontinued
First posted by the FDA
2026-04-22
Presentations affected
2
Manufacturer contact
800-533-4535
Ibrance, Capsule, 100 mg (NDC 0069-0188-21)Discontinuation of the manufacturing of the capsule presentation. 100 mg Tablet NDC 0069-0486-03 will continue to be manufactured.
Ibrance, Capsule, 75 mg (NDC 0069-0187-21)Discontinuation of the manufacturing of the capsule presentation. 75 mg Tablet
NDC 0069-0284-03 will continue to be manufactured.
Dexmedetomidine Hydrochloride Injection
Accord Healthcare Inc.
Anesthesia
2026-04-21
To Be Discontinued
First posted by the FDA
2026-04-21
Presentations affected
1
Manufacturer contact
866-941-7875, option 2
Dexmedetomidine Hydrochloride, Injection, 100 ug/1 mL (NDC 16729-239-93)Discontinuation of the manufacture of the drug
Ketorolac Tromethamine Tablet
Mylan Pharmaceuticals Inc., a Viatris Company
Analgesia/Addiction
2026-04-20
To Be Discontinued
First posted by the FDA
2026-04-20
Presentations affected
1
Manufacturer contact
877-446-3679
Ketorolac Tromethamine, Tablet, 10 mg (NDC 0378-1134-01)Discontinuation of the manufacture of the drug
Rifampin Injection
Sanofi-Aventis U.S. LLC
Anti-Infective
2026-04-20
To Be Discontinued
First posted by the FDA
2026-04-20
Presentations affected
1
Manufacturer contact
800-633-1610
Rifadin, Injection, 600 mg/10 mL (NDC 0068-0597-01)Discontinuation of the manufacture of the drug
Tiagabine Hydrochloride Tablet
Teva Pharmaceuticals USA, Inc.
Neurology
2026-04-15
To Be Discontinued
First posted by the FDA
2026-04-15
Presentations affected
4
Manufacturer contact
888-838-2872
Tiagabine Hydrochloride, Tablet, 12mg 30 count (NDC 0093-8072-56)Discontinuation of the manufacture of the drug
Tiagabine Hydrochloride, Tablet, 16mg 30 count (NDC 0093-8076-56)Discontinuation of the manufacture of the drug
Tiagabine Hydrochloride, Tablet, 2mg 30 count (NDC 0093-5030-56)Discontinuation of the manufacture of the drug
Tiagabine Hydrochloride, Tablet, 4mg 30 count (NDC 0093-5031-56)Discontinuation of the manufacture of the drug
Nitroglycerin Ointment
AbbVie Inc.
Analgesia/Addiction
2026-04-14
To Be Discontinued
First posted by the FDA
2026-04-14
Presentations affected
1
Manufacturer contact
800-678-1605
Rectiv, Ointment, 0.4% (NDC 58914-301-80)Discontinuation of the manufacture of the drug
Nitrofurantoin Oral Suspension
Amneal Pharmaceuticals
Anti-InfectiveOther
2026-04-10
To Be Discontinued
First posted by the FDA
2026-04-10
Presentations affected
1
Manufacturer contact
866-525-7270
Nitrofurantoin, Oral Suspension, 25 mg/5 mL (NDC 69238-2512-9)Discontinuation of the manufacture of the drug
Azithromycin Tablet
Pfizer Inc.
Anti-Infective
2026-04-09
To Be Discontinued
First posted by the FDA
2026-04-09
Presentations affected
2
Manufacturer contact
800-533-4535
Zithromax, Tablet, 250 mg (NDC 0069-4061-01)Discontinuation of the manufacture of the drug
Zithromax, Tablet, 500 mg (NDC 0069-3070-30)Discontinuation of the manufacture of the drug
Aprepitant Oral Powder for Suspension
Merck Sharp & Dohme LLC
Gastroenterology
2026-04-08
To Be Discontinued
First posted by the FDA
2026-04-08
Presentations affected
1
Manufacturer contact
800-672-6372
Emend, Oral Powder for Suspension, 125 mg (NDC 0006-3066-03)To be discontinued in approximately early-September 2026.
Fosaprepitant Dimeglumine Injection
Fresenius Kabi USA, LLC
Gastroenterology
2026-04-08
To Be Discontinued
First posted by the FDA
2026-04-08
Presentations affected
1
Manufacturer contact
888-386-1300
Fosaprepitant Dimeglumine, Injection, 150 mg/5 mL (NDC 63323-972-10)Discontinuation of the manufacture of the drug
Idelalisib Tablet
Gilead Sciences, Inc.
Oncology
2026-04-07
To Be Discontinued
First posted by the FDA
2026-04-07
Presentations affected
2
Manufacturer contact
800-445-3235
Zydelig, Tablet, 100 mg (NDC 61958-1701-1)Discontinuation in the manufacturing of the drug
Zydelig, Tablet, 150 mg (NDC 61958-1702-1)Discontinuation in the manufacturing of the drug
Ursodiol Capsule
Strides Pharma Inc.
Other
2026-04-06
To Be Discontinued
First posted by the FDA
2026-04-06
Presentations affected
1
Manufacturer contact
877-244-9825
Ursodiol, Capsule, 300 mg (NDC 64380-844-06)Discontinuation of the manufacture of the drug
Icosapent Ethyl Capsule
Apotex Corp.
Cardiovascular
2026-04-01
To Be Discontinued
First posted by the FDA
2026-04-01
Presentations affected
2
Manufacturer contact
800-706-5575
Icosapent Ethyl, Capsule, 1 g (NDC 60429-005-12)Discontinuation of the manufacture of the drug
Icosapent Ethyl, Capsule, 1 g (NDC 61474-9711-1)Discontinuation of the manufacture of the drug
Dapsone Gel
Amneal Pharmaceuticals
Dermatology
2026-03-27
To Be Discontinued
First posted by the FDA
2026-03-27
Presentations affected
1
Manufacturer contact
866-525-7270
Dapsone, Gel, 7.5% (NDC 69238-1627-6)Discontinuation of the manufacture of the drug
Progesterone Vaginal Gel
AbbVie Inc.
Urology
2026-03-27
To Be Discontinued
First posted by the FDA
2026-03-27
Presentations affected
1
Manufacturer contact
800-678-1605
Crinone, Vaginal Gel, 4% (NDC 0023-6150-04)Discontinuation of the manufacture of the drug
Tazemetostat Hydrobromide Tablet
Epizyme, Inc. (An Ipsen Company)
Oncology
2026-03-27
To Be Discontinued
First posted by the FDA
2026-03-27
Presentations affected
1
Manufacturer contact
(855)-463-5127
Tazverik, Tablet, 200 mg (NDC 72607-100-00)Discontinuation of the manufacture of the drug product
Clindamycin Palmitate Hydrochloride Injection
Amneal Pharmaceuticals
Anti-Infective
2026-03-26
To Be Discontinued
First posted by the FDA
2026-03-26
Presentations affected
1
Manufacturer contact
866-525-7270
Clindamycin Palmitate Hydrochloride, Injection, 75 mg/5 mL (NDC 53746-468-19)Discontinuation of the manufacture of the drug
Lincomycin Hydrochloride Injection
XGen Pharmaceuticals DJB, Inc.
Anti-Infective
2026-03-26
To Be Discontinued
First posted by the FDA
2026-03-26
Presentations affected
2
Manufacturer contact
866-390-4411
Lincomycin Hydrochloride, Injection, 3 grams/10 mL vial x 10 count (NDC 39822-0355-6)A business decision was made to discontinue manufacture of the drug.
Lincomycin Hydrochloride, Injection, 600 mg/2 mL vial x 10 count (NDC 39822-0350-2)A business decision was made to discontinue manufacture of the drug.
Nebivolol Hydrochloride Tablet
Torrent Pharmaceuticals Limited
Cardiovascular
2026-03-25
To Be Discontinued
First posted by the FDA
2026-03-25
Presentations affected
16
Manufacturer contact
908-280-3333
Nebivolol Hydrochloride, Tablet, 10 mg (NDC 13668-355-01)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 10 mg (NDC 13668-355-05)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 10 mg (NDC 13668-355-30)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 10 mg (NDC 13668-355-90)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 2.5 mg (NDC 13668-353-01)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 2.5 mg (NDC 13668-353-05)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 2.5 mg (NDC 13668-353-30)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 2.5 mg (NDC 13668-353-90)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 20 mg (NDC 13668-356-01)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 20 mg (NDC 13668-356-05)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 20 mg (NDC 13668-356-30)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 20 mg (NDC 13668-356-90)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 5 mg (NDC 13668-354-01)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 5 mg (NDC 13668-354-05)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 5 mg (NDC 13668-354-30)Discontinuation of the manufacture of the drug
Nebivolol Hydrochloride, Tablet, 5 mg (NDC 13668-354-90)Discontinuation of the manufacture of the drug
Ivabradine Hydrochloride Tablet
Amgen Inc.
Cardiovascular
2026-03-24
To Be Discontinued
First posted by the FDA
2026-03-24
Presentations affected
2
Manufacturer contact
1-800-772-6436
Corlanor, Tablet, eq. 5 mg base (NDC 55513-800-60)Discontinuation of the manufacture of the drug product
Corlanor, Tablet, eq. 7.5 mg base (NDC 55513-810-60)Discontinuation of the manufacture of the drug product
Ivabradine Solution
Amgen Inc.
Cardiovascular
2026-03-24
To Be Discontinued
First posted by the FDA
2026-03-24
Presentations affected
1
Manufacturer contact
1-800-772-6436
Corlanor, Solution, 5 mg/5 mL (NDC 55513-813-28)Discontinuation of the manufacture of the drug product
Pilocarpine Hydrochloride Ophthalmic Solution
AbbVie Inc.
Ophthalmology
2026-03-24
To Be Discontinued
First posted by the FDA
2026-03-24
Presentations affected
5
Manufacturer contact
800-633-9110
Vuity, Ophthalmic Solution, 12.5 mg/1 mL (NDC 0074-7098-01)Discontinuation of the manufacture of the drug
Vuity, Ophthalmic Solution, 12.5 mg/1 mL (NDC 0074-7098-03)Discontinuation of the manufacture of the drug
Vuity, Ophthalmic Solution, 12.5 mg/1 mL (NDC 0074-7098-04)Discontinuation of the manufacture of the drug
Vuity, Ophthalmic Solution, 12.5 mg/1 mL (NDC 0074-7098-05)Discontinuation of the manufacture of the drug
Vuity, Ophthalmic Solution, 12.5 mg/1 mL (NDC 0074-7098-06)Discontinuation of the manufacture of the drug
Pentamidine Isethionate Injection
XGen Pharmaceuticals DJB, Inc.
Anti-Infective
2026-03-23
To Be Discontinued
First posted by the FDA
2026-03-23
Presentations affected
1
Manufacturer contact
866-390-4411
Pentamidine Isethionate, Injection, 300 mg/3 mL (NDC 39822-3050-2)A business decision was made to discontinue manufacture of the drug.
Ramelteon Tablet
Takeda Pharmaceuticals USA Inc.
Psychiatry
2026-03-19
To Be Discontinued
First posted by the FDA
2026-03-19
Presentations affected
2
Manufacturer contact
877-825-3327
Rozerem, Tablet, 8 mg (NDC 64764-805-10)Product is expected to be available through February 2027.
Rozerem, Tablet, 8 mg (NDC 64764-805-30)Product is expected to be available through June 2027.
Plerixafor Injection
Fresenius Kabi USA, LLC
Hematology
2026-03-13
To Be Discontinued
First posted by the FDA
2026-03-13
Presentations affected
1
Manufacturer contact
888-391-6300 www.fresenius-kabi.com
Plerixafor, Injection, 24 mg per 1.2 mL (20 mg per mL) (NDC 65219-284-12)A business decision was made to discontinue manufacture of the drug.
Peritoneal Dialysis Solution
Fresenius Medical Care North America
Renal
2026-03-10
To Be Discontinued
First posted by the FDA
2026-03-10
Presentations affected
6
Manufacturer contact
800-323-5188
DELFLEX® w/Dextrose, Solution, 1.5% Low Mg/Low Ca 2.5L/3L, 5/cs (NDC 49230-206-94)The NDC codes are being discontinued, to be replaced with NDC labeler code #46163.
DELFLEX® w/Dextrose, Solution, 1.5% Low Mg/Low Ca 2L, 5/cs (NDC 46163-206-92)The NDC codes are being discontinued, to be replaced with NDC labeler code #46163.
DELFLEX® w/Dextrose, Solution, 2.5% Low Mg/Low Ca 2.5L/3L, 5/cs (NDC 49230-209-94)The NDC codes are being discontinued, to be replaced with NDC labeler code #46163.
DELFLEX® w/Dextrose, Solution, 2.5% Low Mg/Low Ca 2L, 5/cs (NDC 49230-209-92)The NDC codes are being discontinued, to be replaced with NDC labeler code #46163.
DELFLEX® w/Dextrose, Solution, 4.25% Low Mg/Low Ca 2.5L/3L, 5/cs (NDC 46163-212-94)The NDC codes are being discontinued, to be replaced with NDC labeler code #46163.
DELFLEX® w/Dextrose, Solution, 4.25% Low Mg/Low Ca 2L, 5/cs (NDC 46163-212-92)The NDC codes are being discontinued, to be replaced with NDC labeler code #46163.
Everolimus Tablet
Teva Pharmaceuticals USA, Inc.
Transplant
2026-03-02
To Be Discontinued
First posted by the FDA
2026-03-02
Presentations affected
4
Manufacturer contact
800-545-8800
Everolimus, Tablet, 10 mg (NDC 0093-7769-24)Discontinuation of the manufacture of the drug
Everolimus, Tablet, 2.5 mg (NDC 0093-7766-24)Discontinuation of the manufacture of the drug
Everolimus, Tablet, 5 mg (NDC 0093-7767-24)Discontinuation of the manufacture of the drug
Everolimus, Tablet, 7.5 mg (NDC 0093-7768-24)Discontinuation of the manufacture of the drug
Itraconazole Capsule
Janssen Pharmaceuticals
Anti-InfectiveOther
2026-02-27
To Be Discontinued
First posted by the FDA
2026-02-27
Presentations affected
3
Manufacturer contact
800-JANSSEN (1-800-526-7736)
Sporanox, Capsule, 100 mg (NDC 10147-1700-3)Discontinuation of the manufacture of the drug
Sporanox, Capsule, 100 mg (NDC 50458-290-01)Discontinuation of the manufacture of the drug
Sporanox, Capsule, 100 mg (NDC 50458-290-04)Discontinuation of the manufacture of the drug
Clindamycin Hydrochloride Capsule
Pfizer Inc.
Anti-Infective
2026-02-25
To Be Discontinued
First posted by the FDA
2026-02-25
Presentations affected
3
Manufacturer contact
844-646-4398
Cleocin Hydrochloride, Capsule, 150 mg (NDC 0009-0225-02)Discontinuation of the manufacture of the drug
Cleocin Hydrochloride, Capsule, 300 mg (NDC 0009-0395-14)Discontinuation of the manufacture of the drug
Cleocin Hydrochloride, Capsule, 75 mg (NDC 0009-0331-02)Discontinuation of the manufacture of the drug
Lincomycin Hydrochloride Injection
Pfizer Inc.
Anti-Infective
2026-02-25
To Be Discontinued
First posted by the FDA
2026-02-25
Presentations affected
1
Manufacturer contact
844-646-4398
Lincocin, Injection, 2 mL multiple dose vial (NDC 0009-0104-04)Discontinuation of the manufacture of the drug
Oxaliplatin Injection
Fresenius Kabi USA, LLC
Oncology
2026-02-25
To Be Discontinued
First posted by the FDA
2026-02-25
Presentations affected
2
Manufacturer contact
847-550-2300
Oxaliplatin, Injection, 5 mg/mL (NDC 63323-750-10)A business decision was made to discontinue manufacture of the drug.
Oxaliplatin, Injection, 5 mg/mL (NDC 63323-750-20)A business decision was made to discontinue manufacture of the drug.
Arsenic Trioxide Injection
Ingenus Pharmaceuticals LLC
Oncology
2026-02-24
To Be Discontinued
First posted by the FDA
2026-02-24
Presentations affected
1
Manufacturer contact
866-321-5031
Arsenic Trioxide, Injection, 1 mg/1 mL (NDC 50742-438-10)A business decision was made to discontinue manufacture of the drug.
Frovatriptan Succinate Tablet
Endo Pharmaceuticals, Inc.
Neurology
2026-02-24
To Be Discontinued
First posted by the FDA
2025-11-12
Presentations affected
2
Manufacturer contact
800-828-9393
Frova, Tablet, 2.5 mg (NDC 63481-025-09)A business decision was made to discontinue manufacture of the drug.
Frova, Tablet, 2.5 mg (NDC 0603-3718-34)A business decision was made to discontinue manufacture of the drug.
Irinotecan Hydrochloride Injection
Ingenus Pharmaceuticals LLC
Oncology
2026-02-24
To Be Discontinued
First posted by the FDA
2026-02-24
Presentations affected
2
Manufacturer contact
866-321-5031
Irinotecan Hydrochloride, Injection, 100 mg/5 mL (NDC 50742-402-05)A business decision was made to discontinue manufacture of the drug.
Irinotecan Hydrochloride, Injection, 40 mg/2 mL (NDC 50742-401-02)A business decision was made to discontinue manufacture of the drug.
Carboplatin Injection
Ingenus Pharmaceuticals LLC
Oncology
2026-02-20
To Be Discontinued
First posted by the FDA
2026-02-20
Presentations affected
2
Manufacturer contact
866-321-5031
Carboplatin, Injection, 450 mg/45 mL (NDC 50742-447-45)Discontinuation of the manufacture of the drug
Carboplatin, Injection, 600 mg/60 mL (NDC 50742-448-60)Discontinuation of the manufacture of the drug
Decitabine Injection
Ingenus Pharmaceuticals LLC
Oncology
2026-02-20
To Be Discontinued
First posted by the FDA
2026-02-20
Presentations affected
2
Manufacturer contact
866-321-5031
Decitabine, Injection, 50 mg (NDC 50742-430-01)Discontinuation of the manufacture of the drug
Decitabine, Injection, 50 mg (NDC 68001-573-41)Labeler: BluePoint Laboratories; Discontinuation of the manufacture of the drug
Docetaxel Injection
Ingenus Pharmaceuticals LLC
Oncology
2026-02-20
To Be Discontinued
First posted by the FDA
2026-02-20
Presentations affected
2
Manufacturer contact
866-321-5031
Docetaxel, Injection, 10 mg/1 mL (NDC 50742-431-08)A business decision was made to discontinue manufacture of the drug.
Docetaxel, Injection, 10 mg/1 mL (NDC 50742-463-16)A business decision was made to discontinue manufacture of the drug.
Allopurinol Tablet
Teva Pharmaceuticals USA, Inc.
OncologyRenalRheumatology
2026-02-19
To Be Discontinued
First posted by the FDA
2026-02-19
Presentations affected
4
Manufacturer contact
800-545-8800
Allopurinol, Tablet, 100 mg (NDC 0591-5543-01)Discontinuation of the manufacture of the drug
Allopurinol, Tablet, 100 mg (NDC 0591-5543-10)Discontinuation of the manufacture of the drug
Allopurinol, Tablet, 300 mg (NDC 0591-5544-01)Discontinuation of the manufacture of the drug
Allopurinol, Tablet, 300 mg (NDC 0591-5544-05)Discontinuation of the manufacture of the drug
Cefepime Hydrochloride Injection
Fresenius Kabi USA, LLC
Anti-Infective
2026-02-10
To Be Discontinued
First posted by the FDA
2026-02-10
Presentations affected
2
Manufacturer contact
888-386-1300
Cefepime Hydrochloride, Injection, 1 g (NDC 63323-326-20)Discontinuation of the manufacture of the drug.
Cefepime Hydrochloride, Injection, 2 g (NDC 63323-340-20)Discontinuation of the manufacture of the drug.
Chlorothiazide Oral Suspension
Salix Pharmaceuticals, a division of Bausch Health US, LLC
Lopid, Tablet, 600 mg (NDC 0071-0737-20)Discontinuation of the manufacture of the drug.
Pindolol Tablet
Sun Pharmaceutical Industries, Inc.
Cardiovascular
2026-01-30
To Be Discontinued
First posted by the FDA
2026-01-30
Presentations affected
2
Manufacturer contact
800-818-4555
Pindolol, Tablet, 10 mg (NDC 57664-656-88)Discontinuation of the manufacture of the drug; Expiry date of last distributed batch October 2026
Pindolol, Tablet, 5 mg (NDC 57664-655-88)Discontinuation of the manufacture of the drug; Expiry date of last distributed batch January 2027
Podofilox Topical Gel
AbbVie Inc.
DermatologyOther
2026-01-28
To Be Discontinued
First posted by the FDA
2026-01-28
Presentations affected
1
Manufacturer contact
800-633-9110
Condylox , Topical Gel, 0.5% (NDC 0023-6118-03)Discontinuation of the manufacture of the drug
Benztropine Mesylate Injection
Fresenius Kabi USA, LLC
Neurology
2026-01-27
To Be Discontinued
First posted by the FDA
2026-01-27
Presentations affected
1
Manufacturer contact
888-386-1300
Benztropine Mesylate, Injection, 1 mg/1 mL (NDC 63323-970-02)Discontinuation of the manufacture of the drug
Fluvastatin Sodium Tablet, Extended Release
Sandoz Inc.
Cardiovascular
2026-01-27
To Be Discontinued
First posted by the FDA
2026-01-27
Presentations affected
3
Manufacturer contact
800-525-8747
Fluvastatin Sodium, Tablet, Extended Release, 80 mg (NDC 0781-8017-01)Discontinuation of the manufacture of the drug
Fluvastatin Sodium, Tablet, Extended Release, 80 mg (NDC 0781-8017-31)Discontinuation of the manufacture of the drug
Lescol XL, Tablet, Extended Release, 80 mg (NDC 66758-211-31)Discontinuation of the manufacture of the drug
Azithromycin Injection
Pfizer Inc.
Anti-Infective
2026-01-20
To Be Discontinued
First posted by the FDA
2026-01-20
Presentations affected
1
Manufacturer contact
844-646-4398
Zithromax IV, Injection, 500 mg/5 mL (NDC 0069-3150-83)Discontinuation of the manufacture of the drug.
Maraviroc Solution
ViiV Healthcare Company
Antiviral
2026-01-20
To Be Discontinued
First posted by the FDA
2026-01-20
Presentations affected
1
Manufacturer contact
877-844-8872
Selzentry, Solution, 20 mg/mL Oral Solution Kit | 230 mL Oral Solution per Bottle | 1 Bottle per Carton (NDC 49702-260-55)The anticipated date that GSK will cease distribution of the product is approximately August 1, 2026.
Piperacillin and Tazobactam Injection
Fresenius Kabi USA, LLC
Anti-Infective
2026-01-20
To Be Discontinued
First posted by the FDA
2026-01-20
Presentations affected
1
Manufacturer contact
888-386-1300
Piperacillin and Tazobactam, Injection, 2.25 g vial (NDC 65219-434-20)Discontinuation of the manufacture of the drug
Riboflavin 5-phosphate Ophthalmic Solution
Glaukos Corporation
Ophthalmology
2026-01-20
To Be Discontinued
First posted by the FDA
2026-01-20
Presentations affected
1
Manufacturer contact
949-367-9600
Photrexa Cross-linking Kit, Ophthalmic Solution, Kit (NDC 25357-025-03)Discontinuing manufacture of the product as of July 2026.
Adalimumab-adaz Injection
Sandoz Inc.
Rheumatology
2026-01-13
To Be Discontinued
First posted by the FDA
2026-01-13
Presentations affected
5
Manufacturer contact
800-525-8747
Hyrimoz, Injection, 40 mg/.4 mL (NDC 61314-473-64)Equivalent Sandoz format is available.
Hyrimoz, Injection, 80 mg/.8 mL (NDC 61314-454-36)Equivalent Sandoz format is available.
Hyrimoz, Injection, 80 mg/.8 mL (NDC 61314-454-68)Equivalent Sandoz format is available.
Hyrimoz, Injection, Kit (NDC 61314-517-36)Equivalent Sandoz format is available.
Hyrimoz, Injection, Kit (NDC 61314-531-64)Equivalent Sandoz format is available.
Caspofungin Acetate Injection
Fresenius Kabi USA, LLC
Anti-Infective
2026-01-12
To Be Discontinued
First posted by the FDA
2026-01-12
Presentations affected
1
Manufacturer contact
888-386-1300
Caspofungin Acetate, Injection, 7 mg/1 mL (NDC 63323-358-10)Discontinuation of the manufacture of the drug
Doxycycline Hyclate Tablet
Mylan Pharmaceuticals Inc., a Viatris Company
Anti-Infective
2026-01-12
To Be Discontinued
First posted by the FDA
2026-01-12
Presentations affected
2
Manufacturer contact
800-796-9526
Doxycycline Hyclate, Tablet, 100 mg (NDC 0378-0167-02)Discontinuation of the manufacture of the drug
Doxycycline Hyclate, Tablet, 100 mg (NDC 0378-0167-13)Discontinuation of the manufacture of the drug
Doxylamine Succinate and Pyridoxine Hydrochloride Tablet, Delayed Release
Mylan Pharmaceuticals Inc., a Viatris Company
Other
2026-01-12
To Be Discontinued
First posted by the FDA
2026-01-12
Presentations affected
1
Manufacturer contact
800-796-9526
Doxylamine Succinate and Pyridoxine Hydrochloride, Tablet, Delayed Release, 10 mg; 10 mg (NDC 0378-4615-01)A business decision was made to discontinue manufacture of the drug.
Neostigmine Methylsulfate Injection
Fresenius Kabi USA, LLC
Analgesia/Addiction
2026-01-12
To Be Discontinued
First posted by the FDA
2026-01-12
Presentations affected
1
Manufacturer contact
888-386-1300
Neostigmine Methylsulfate, Injection, .5 mg/1 mL (NDC 63323-413-10)Discontinuation of the manufacture of the drug
Haloperidol Decanoate Injection
Fresenius Kabi USA, LLC
Psychiatry
2026-01-09
To Be Discontinued
First posted by the FDA
2026-01-09
Presentations affected
2
Manufacturer contact
888-386-1300
Haloperidol Decanoate, Injection, 50 mg/1 mL (NDC 63323-469-01)Discontinuation of the manufacture of the drug
Haloperidol Decanoate, Injection, 50 mg/1 mL (NDC 63323-469-05)Discontinuation of the manufacture of the drug
Imipenem and Cilastatin Injection
Merck Sharp & Dohme Corp.
Anti-Infective
2026-01-08
To Be Discontinued
First posted by the FDA
2026-01-08
Presentations affected
1
Manufacturer contact
800-672-6372
Primaxin, Injection, 500mg (NDC 0006-3516-59)To be discontinued approximately 11/30/2026
Everolimus Tablet
Endo Pharmaceuticals, Inc.
Transplant
2026-01-06
To Be Discontinued
First posted by the FDA
2026-01-06
Presentations affected
4
Manufacturer contact
800-828-9393
Everolimus, Tablet, 10 mg (NDC 49884-128-91)Discontinuation of the manufacture of the drug
Everolimus, Tablet, 2.5 mg (NDC 49884-119-91)Discontinuation of the manufacture of the drug
Everolimus, Tablet, 5 mg (NDC 49884-125-91)Discontinuation of the manufacture of the drug
Everolimus, Tablet, 7.5 mg (NDC 49884-127-91)Discontinuation of the manufacture of the drug
Diltiazem Hydrochloride Injection
Hospira, Inc., a Pfizer Company
Cardiovascular
2026-01-05
To Be Discontinued
First posted by the FDA
2026-01-05
Presentations affected
1
Manufacturer contact
844-646-4398
Diltiazem Hydrochloride, Injection, 100 mg Single Dose ADD-Vantage® Glass Vial (NDC 0409-4350-03)Discontinuation of the manufacture of the drug
Hydroxychloroquine Sulfate Tablet
Teva Pharmaceuticals USA, Inc.
Anti-InfectiveOtherRheumatology
2026-01-05
To Be Discontinued
First posted by the FDA
2026-01-05
Presentations affected
1
Manufacturer contact
800-545-8800
Hydroxychloroquine Sulfate, Tablet, 200 mg (NDC 0093-2401-01)Discontinuation of the manufacture of the drug
Sodium Oxybate Solution
Amneal Pharmaceuticals
Psychiatry
2025-12-29
To Be Discontinued
First posted by the FDA
2025-12-29
Presentations affected
1
Manufacturer contact
800-525-7270
Sodium Oxybate, Solution, .5 g/1 mL (NDC 69238-2391-1)Discontinuation of the manufacture of the drug
Mirikizumab-mrkz Injection
Eli Lilly and Co.
GastroenterologyOther
2025-12-22
To Be Discontinued
First posted by the FDA
2025-12-22
Presentations affected
2
Manufacturer contact
800-545-5979
Omvoh, Injection, 100 mg/1 mL (NDC 0002-8011-27)A business decision was made to discontinue. Distribution will end April 2026. The 200 mg/2 mL injection presentation (NDC 0002-3116-11) will remain.
Omvoh, Injection, 100 mg/1 mL (NDC 0002-8870-27)A business decision was made to discontinue. Distribution will end April 2026. The 200 mg/2 mL injection presentation (NDC 0002-1442-11) will remain.
Morphine Sulfate Tablet
Upsher-Smith Laboratories, LLC
Analgesia/Addiction
2025-12-22
To Be Discontinued
First posted by the FDA
2025-12-22
Presentations affected
2
Manufacturer contact
763-315-2000
Morphine Sulfate, Tablet, 15 mg (NDC 0832-0273-11)Discontinuation of the manufacture of the drug
Morphine Sulfate, Tablet, 30 mg (NDC 0832-0274-11)Discontinuation of the manufacture of the drug
Carbamazepine Capsule, Extended Release
Takeda Pharmaceuticals USA Inc.
Neurology
2025-12-19
To Be Discontinued
First posted by the FDA
2025-12-19
Presentations affected
3
Manufacturer contact
855-268-1825
Carbatrol, Capsule, Extended Release, 100 mg (NDC 54092-171-12)Discontinuation of the manufacture of the drug
Carbatrol, Capsule, Extended Release, 200 mg (NDC 54092-172-12)Discontinuation of the manufacture of the drug
Carbatrol, Capsule, Extended Release, 300 mg (NDC 54092-173-12)Discontinuation of the manufacture of the drug
Doxercalciferol Injection
Sanofi-Aventis U.S. LLC
Endocrinology/Metabolism
2025-12-10
To Be Discontinued
First posted by the FDA
2025-12-10
Presentations affected
3
Manufacturer contact
800-633-1610
Hectorol, Injection, 2 mcg/mL injection 50 single-dose vials (NDC 58468-0126-1)Discontinuation of the manufacture of the drug
Hectorol, Injection, 4 mcg/2 mL injection 50 multiple-dose vials (NDC 58468-0127-1)Discontinuation of the manufacture of the drug
Hectorol, Injection, 4 mcg/2 mL injection 50 single-dose vials (NDC 58468-0123-1)Discontinuation of the manufacture of the drug
Spironolactone Tablet
Pfizer Inc.
Cardiovascular
2025-12-10
To Be Discontinued
First posted by the FDA
2025-12-10
Presentations affected
2
Manufacturer contact
800-533-4535
Aldactone, Tablet, 100 mg (NDC 0025-1031-31)Discontinuation of the manufacture of the drug.
Aldactone, Tablet, 25 mg (NDC 0025-1001-31)Discontinuation of the manufacture of the drug.
Ampicillin Sodium Injection
Sandoz Inc.
Anti-Infective
2025-12-08
To Be Discontinued
First posted by the FDA
2025-12-08
Presentations affected
5
Manufacturer contact
800-525-8747
Ampicillin Sodium, Injection, 1 g (NDC 0781-9404-95)Discontinuation of private label only
Ampicillin Sodium, Injection, 1 g (NDC 0781-9412-92)Discontinuation of private label only
Ampicillin Sodium, Injection, 10 g (NDC 0781-9409-95)Discontinuation of private label only
Ampicillin Sodium, Injection, 2 g (NDC 0781-9408-95)Discontinuation of private label only
Ampicillin Sodium, Injection, 2 g (NDC 0781-9413-92)Discontinuation of private label only
Calcitriol Capsule
Teva Pharmaceuticals USA, Inc.
Endocrinology/Metabolism
2025-12-04
To Be Discontinued
First posted by the FDA
2025-12-04
Presentations affected
2
Manufacturer contact
800-545-8800
Calcitriol, Capsule, .25 ug (NDC 0093-7352-01)A business decision was made to discontinue manufacture of the drug
Calcitriol, Capsule, .5 ug (NDC 0093-7353-01)A business decision was made to discontinue manufacture of the drug
Sodium Chloride 0.9% Injection
Hospira, Inc., a Pfizer Company
GastroenterologyOtherRenal
2025-12-03
To Be Discontinued
First posted by the FDA
2025-12-03
Presentations affected
3
Manufacturer contact
844-646-4398
Sodium Chloride 0.9%, Injection, 100 mL ADD-Vantage® Flexible Container (NDC 0409-7101-67)Discontinuation of the manufacture of the drug
Sodium Chloride 0.9%, Injection, 250 mL ADD-Vantage® Flexible Container (NDC 0409-7101-02)Discontinuation of the manufacture of the drug
Sodium Chloride 0.9%, Injection, 50 mL ADD-Vantage® Flexible Container (NDC 0409-7101-66)Discontinuation of the manufacture of the drug
Posaconazole Injection
Merck Sharp & Dohme Corp.
Anti-Infective
2025-12-02
To Be Discontinued
First posted by the FDA
2025-12-02
Presentations affected
1
Manufacturer contact
800-672-6372
Noxafil, Injection, 18 mg/1 mL (NDC 0085-4331-01)Discontinuation of the manufacture of the drug
Nilutamide Tablet
Advanz Pharma (US) Corp.
Oncology
2025-12-01
To Be Discontinued
First posted by the FDA
2025-12-01
Presentations affected
2
Manufacturer contact
847-283-7921
Nilandron, Tablet, 150 mg (NDC 59212-111-14)Product to expire in March 2026; Discontinuation of the manufacture of the drug
Nilandron, Tablet, 150 mg (NDC 66993-212-38)Product to expire in March 2026; Discontinuation of the manufacture of the drug
Phenoxybenzamine Hydrochloride Capsule
Advanz Pharma (US) Corp.
Cardiovascular
2025-12-01
To Be Discontinued
First posted by the FDA
2025-12-01
Presentations affected
3
Manufacturer contact
847-283-7921
Dibenzyline, Capsule, 10 mg (NDC 59212-001-01)Discontinuation of the manufacture of the drug
Dibenzyline, Capsule, 10 mg (NDC 59212-001-02)Discontinuation of the manufacture of the drug
Dibenzyline, Capsule, 10 mg (NDC 66993-066-02)Discontinuation of the manufacture of the drug
Potassium Chloride Tablet, Extended Release
Teva Pharmaceuticals USA, Inc.
Endocrinology/MetabolismGastroenterology
2025-11-21
To Be Discontinued
First posted by the FDA
2025-11-21
Presentations affected
4
Manufacturer contact
800-545-8800
Potassium Chloride, Tablet, Extended Release, 10 meq (NDC 62037-710-01)Discontinuation of the manufacture of the drug
Potassium Chloride, Tablet, Extended Release, 20 meq (NDC 62037-720-01)Discontinuation of the manufacture of the drug
Potassium Chloride, Tablet, Extended Release, 20 meq (NDC 62037-720-05)Discontinuation of the manufacture of the drug
Potassium Chloride, Tablet, Extended Release, 20 meq (NDC 62037-720-10)Discontinuation of the manufacture of the drug
Verapamil Hydrochloride Injection
Pfizer Inc.
Cardiovascular
2025-11-21
To Be Discontinued
First posted by the FDA
2025-11-21
Presentations affected
1
Manufacturer contact
844-646-4398
Verapamil Hydrochloride, Injection, 2.5 mg/1 mL (NDC 0409-9633-05)Discontinuation of the manufacture of the drug
Anagrelide Hydrochloride Capsule
Teva Pharmaceuticals USA, Inc.
Hematology
2025-11-19
To Be Discontinued
First posted by the FDA
2025-11-19
Presentations affected
2
Manufacturer contact
800-545-8800
Anagrelide Hydrochloride, Capsule, 0.5 mg (NDC 0172-5241-60)A business decision was made to discontinue manufacture of the drug.
Anagrelide Hydrochloride, Capsule, 1 mg (NDC 0172-5240-60)A business decision was made to discontinue manufacture of the drug.
Hydrochlorothiazide Capsule
Teva Pharmaceuticals USA, Inc.
Cardiovascular
2025-11-19
To Be Discontinued
First posted by the FDA
2025-11-19
Presentations affected
2
Manufacturer contact
800-545-8800
Microzide, Capsule, 12.5 mg (NDC 0591-0347-01)A business decision was made to discontinue manufacture of the drug.
Microzide, Capsule, 12.5 mg (NDC 0591-0347-05)A business decision was made to discontinue manufacture of the drug.
Valsartan Tablet
Mylan Pharmaceuticals Inc., a Viatris Company
Cardiovascular
2025-11-19
To Be Discontinued
First posted by the FDA
2025-11-19
Presentations affected
4
Manufacturer contact
800-796-9526
Valsartan, Tablet, 160 mg (NDC 0378-5814-77)A business decision was made to discontinue manufacture of the drug.
Valsartan, Tablet, 320 mg (NDC 0378-5815-77)A business decision was made to discontinue manufacture of the drug.
Valsartan, Tablet, 40 mg (NDC 0378-5807-93)A business decision was made to discontinue manufacture of the drug.
Valsartan, Tablet, 80 mg (NDC 0378-5813-77)A business decision was made to discontinue manufacture of the drug.
Montelukast Sodium Tablet, Chewable
Organon
Pulmonary/Allergy
2025-11-17
To Be Discontinued
First posted by the FDA
2025-11-17
Presentations affected
1
Manufacturer contact
844-674-3200
Singulair, Tablet, Chewable, 4 mg (NDC 78206-170-01)Discontinuation of the manufacture of the drug
Ceftazidime Injection
Hospira, Inc., a Pfizer Company
Anti-Infective
2025-11-14
To Be Discontinued
First posted by the FDA
2025-11-14
Presentations affected
2
Manufacturer contact
844-646-4398
Tazicef, Injection, 1 g (NDC 0409-5092-16)Discontinuation of the manufacture of the drug
Tazicef, Injection, 2 g (NDC 0409-5093-11)Discontinuation of the manufacture of the drug
Palonosetron Hydrochloride Injection
Teva Pharmaceuticals USA, Inc.
Gastroenterology
2025-11-14
To Be Discontinued
First posted by the FDA
2025-11-14
Presentations affected
1
Manufacturer contact
800-545-8800
Palonosetron Hydrochloride, Injection, .25 mg/5 mL (NDC 0703-4094-01)Discontinuation of the manufacture of the drug
Somatropin Injection
Novo Nordisk, Inc.
Endocrinology/Metabolism
2025-11-14
To Be Discontinued
First posted by the FDA
2025-11-14
Presentations affected
1
Manufacturer contact
833-493-4689
Norditropin, Injection, 30 mg/3 mL (NDC 0169-7703-21)Discontinuation of the manufacture of the drug
Vancomycin Hydrochloride Injection
Hospira, Inc., a Pfizer Company
Anti-Infective
2025-11-14
To Be Discontinued
First posted by the FDA
2025-11-14
Presentations affected
1
Manufacturer contact
844-646-4398
Vancomycin Hydrochloride, Injection, 10 g Vial NovaPlus (NDC 0409-5017-01)Discontinuation of the manufacture of the drug
Adalimumab-ryvk Kit
Teva Pharmaceuticals USA, Inc.
Rheumatology
2025-11-13
To Be Discontinued
First posted by the FDA
2025-11-13
Presentations affected
1
Manufacturer contact
800-545-8800
Simlandi, Kit, Kit (NDC 51759-523-21)Discontinuation of the manufacture of the drug
Cetrorelix Acetate Injection
Teva Pharmaceuticals USA, Inc.
Reproductive
2025-11-13
To Be Discontinued
First posted by the FDA
2025-11-13
Presentations affected
1
Manufacturer contact
800-545-8800
Cetrorelix Acetate, Injection, Kit (NDC 0480-5795-08)Discontinuation of the manufacture of the drug
Guanfacine Hydrochloride Tablet, Extended Release
Actavis Pharma, Inc.
Psychiatry
2025-11-13
To Be Discontinued
First posted by the FDA
2025-11-13
Presentations affected
4
Manufacturer contact
800-545-8800
Guanfacine Hydrochloride, Tablet, Extended Release, 1 mg (NDC 0228-2850-11)A business decision was made to discontinue manufacture of the drug.
Guanfacine Hydrochloride, Tablet, Extended Release, 2 mg (NDC 0228-2851-11)A business decision was made to discontinue manufacture of the drug.
Guanfacine Hydrochloride, Tablet, Extended Release, 3 mg (NDC 0228-2853-11)A business decision was made to discontinue manufacture of the drug.
Guanfacine Hydrochloride, Tablet, Extended Release, 4 mg (NDC 0228-2855-11)A business decision was made to discontinue manufacture of the drug.
Atropine Sulfate Injection
Hospira, Inc., a Pfizer Company
AnesthesiaNeurologyPediatric
2025-11-07
To Be Discontinued
First posted by the FDA
2025-11-07
Presentations affected
2
Manufacturer contact
844-646-4398
Atropine Sulfate, Injection, (Adult) 0.5 mg/5 mL (0.1 mg/mL) LifeShield® ABBOJECT® Glass Syringe (20 G x 1 1/2) (NDC 0409-4910-34)"Discontinuation of the manufacture of the drug
Atropine Sulfate, Injection, (Adult)1 mg/10 mL (0.1 mg/mL) LifeShield® ABBOJECT® Glass Syringe (20 G x 1 1/2) (NDC 0409-4911-34)"Discontinuation of the manufacture of the drug
Calcium Chloride Injection
Hospira, Inc., a Pfizer Company
CardiovascularEndocrinology/Metabolism
2025-11-07
To Be Discontinued
First posted by the FDA
2025-11-07
Presentations affected
1
Manufacturer contact
844-646-4398
Calcium Chloride, Injection, 100 mg/1 mL (NDC 0409-4928-34)Discontinuation of the manufacture of the drug
Deferiprone Tablet
Chiesi USA, Inc.
Hematology
2025-11-07
To Be Discontinued
First posted by the FDA
2025-11-07
Presentations affected
1
Manufacturer contact
888-466-6505
Ferriprox, Tablet, 500 mg (NDC 10122-100-10)Discontinuation of the manufacture of the drug.
Dextrose Monohydrate 50% Injection
Hospira, Inc., a Pfizer Company
Endocrinology/MetabolismGastroenterologyPediatric
2025-11-07
To Be Discontinued
First posted by the FDA
2025-11-07
Presentations affected
1
Manufacturer contact
844-646-4398
Dextrose Monohydrate 50%, Injection, 50% Dextrose Injection 0.5 g/mL; ABBOJECT® Glass Syringe (NDC 0409-4902-34)Discontinuation of the manufacture of the drug
Epinephrine Injection
Hospira, Inc., a Pfizer Company
CardiovascularEndocrinology/Metabolism
2025-11-07
To Be Discontinued
First posted by the FDA
2025-11-07
Presentations affected
2
Manufacturer contact
844-646-4398
Epinephrine, Injection, .1 mg/1 mL (NDC 0409-4933-01)Discontinuation of the manufacture of the drug
Epinephrine, Injection, .1 mg/1 mL (NDC 0409-4933-10)Discontinuation of the manufacture of the drug
Ketamine Hydrochloride Injection
Pfizer Inc.
Anesthesia
2025-11-07
To Be Discontinued
First posted by the FDA
2025-11-07
Presentations affected
1
Manufacturer contact
844-646-4398
Ketamine Hydrochloride, Injection, 500 mg/5mL (100 mg/mL); Multiple Dose Glass Fliptop Vial Novaplus (NDC 0409-0040-10)Discontinuation of the manufacture of the drug
Lidocaine Hydrochloride Injection
Hospira, Inc., a Pfizer Company
Analgesia/AddictionAnesthesiaPediatric
2025-11-07
To Be Discontinued
First posted by the FDA
2025-11-07
Presentations affected
2
Manufacturer contact
844-646-4398
Lidocaine Hydrochloride, Injection, 1%, USP (For Cardiac Use Only) 50 mg/5 mL (10 mg/mL) LifeShield™ ABBOJECT® Glass Syringe (20 G x 1 1/2) (NDC 0409-4904-34)"Discontinuation of the manufacture of the drug
Lidocaine Hydrochloride, Injection, 2%, USP (For Cardiac Use Only) 100 mg/5 mL (20 mg/mL) LifeShield® ABBOJECT® Glass Syringe (20 G x 1 1/2) (NDC 0409-4903-34)"Discontinuation of the manufacture of the drug
Sodium Bicarbonate Injection
Hospira, Inc., a Pfizer Company
Endocrinology/MetabolismGastroenterologyPediatric
2025-11-07
To Be Discontinued
First posted by the FDA
2025-11-07
Presentations affected
4
Manufacturer contact
844-646-4398
Sodium Bicarbonate, Injection, 42 mg/1 mL (NDC 0409-5534-14)Discontinuation of the manufacture of the drug
Sodium Bicarbonate, Injection, 75 mg/1 mL (NDC 0409-4916-14)Discontinuation of the manufacture of the drug
Sodium Bicarbonate, Injection, 84 mg/1 mL (NDC 0409-4900-14)Discontinuation of the manufacture of the drug
Sodium Bicarbonate, Injection, 84 mg/1 mL (NDC 0409-6637-14)Discontinuation of the manufacture of the drug
Acetaminophen; Oxycodone Hydrochloride Tablet
Endo Pharmaceuticals, Inc.
Analgesia/Addiction
2025-11-03
To Be Discontinued
First posted by the FDA
2025-11-03
Presentations affected
6
Manufacturer contact
800-828-9393
Acetaminophen; Oxycodone Hydrochloride, Tablet, 325 mg; 10 mg (NDC 60951-712-70)Discontinuation of the manufacture of the drug
Acetaminophen; Oxycodone Hydrochloride, Tablet, 325 mg; 2.5 mg (NDC 60951-701-70)Discontinuation of the manufacture of the drug
Acetaminophen; Oxycodone Hydrochloride, Tablet, 325 mg; 2.5 mg (NDC 63481-627-70)Discontinuation of the manufacture of the drug
Acetaminophen; Oxycodone Hydrochloride, Tablet, 325 mg; 5 mg (NDC 60951-602-70)Discontinuation of the manufacture of the drug
Acetaminophen; Oxycodone Hydrochloride, Tablet, 325 mg; 5 mg (NDC 60951-602-85)Discontinuation of the manufacture of the drug
Acetaminophen; Oxycodone Hydrochloride, Tablet, 325 mg; 7.5 mg (NDC 60951-700-70)Discontinuation of the manufacture of the drug
Atazanavir Sulfate; Cobicistat Tablet
Bristol Myers Squibb Co.
Antiviral
2025-11-03
To Be Discontinued
First posted by the FDA
2025-11-03
Presentations affected
1
Manufacturer contact
800-332-2056
Evotaz, Tablet, 300 mg; 150 mg (NDC 0003-3641-11)The global Cease Manufacture date for EVOTAZ® currently is estimated to begin April 2026.
Everolimus Tablet
Mylan Pharmaceuticals Inc., a Viatris Company
Transplant
2025-11-03
To Be Discontinued
First posted by the FDA
2025-11-03
Presentations affected
3
Manufacturer contact
800-796-9526
Everolimus, Tablet, 2 mg (NDC 0378-0005-85)Discontinuation of the manufacture of the drug
Everolimus, Tablet, 3 mg (NDC 0378-0006-85)Discontinuation of the manufacture of the drug
Everolimus, Tablet, 5 mg (NDC 0378-0007-85)Discontinuation of the manufacture of the drug
Lasmiditan Succinate Tablet
Eli Lilly and Co.
Neurology
2025-11-03
To Be Discontinued
First posted by the FDA
2025-11-03
Presentations affected
6
Manufacturer contact
800-545-5979
Reyvow, Tablet, 100 mg (NDC 0002-4491-08)A business decision was made to discontinue manufacture of the 50 mg and 100 mg tablets. Distribution will end on May 31, 2026.
Reyvow, Tablet, 100 mg (NDC 0002-4491-61)A business decision was made to discontinue manufacture of the 50 mg and 100 mg tablets. Distribution will end on May 31, 2026.
Reyvow, Tablet, 100 mg (NDC 0002-4491-62)A business decision was made to discontinue manufacture of the 50 mg and 100 mg tablets. Distribution will end on May 31, 2026.
Reyvow, Tablet, 50 mg (NDC 0002-4312-08)A business decision was made to discontinue manufacture of the 50 mg and 100 mg tablets. Distribution will end on May 31, 2026.
Reyvow, Tablet, 50 mg (NDC 0002-4312-61)A business decision was made to discontinue manufacture of the 50 mg and 100 mg tablets. Distribution will end on May 31, 2026.
Reyvow, Tablet, 50 mg (NDC 0002-4312-62)A business decision was made to discontinue manufacture of the 50 mg and 100 mg tablets. Distribution will end on May 31, 2026.
Scopolamine Transdermal System
Padagis US LLC
GastroenterologyNeurologyOther
2025-11-03
To Be Discontinued
First posted by the FDA
2025-11-03
Presentations affected
1
Manufacturer contact
866-634-9120
Scopolamine, Transdermal System, 1 mg (NDC 45802-580-46)Discontinuation of the manufacture of the drug
Phenobarbital Tablet
Endo Pharmaceuticals, Inc.
Analgesia/AddictionNeurologyOther
2025-10-31
To Be Discontinued
First posted by the FDA
2025-10-31
Presentations affected
8
Manufacturer contact
800-828-9393
Phenobarbital, Tablet, 16.2 mg (NDC 0603-5165-21)Discontinuation of the manufacture of the drug
Phenobarbital, Tablet, 16.2 mg (NDC 0603-5165-32)Discontinuation of the manufacture of the drug
Phenobarbital, Tablet, 32.4 mg (NDC 0603-5166-21)Discontinuation of the manufacture of the drug
Phenobarbital, Tablet, 32.4 mg (NDC 0603-5166-32)Discontinuation of the manufacture of the drug
Phenobarbital, Tablet, 64.8 mg (NDC 0603-5167-21)Discontinuation of the manufacture of the drug
Phenobarbital, Tablet, 64.8 mg (NDC 0603-5167-32)Discontinuation of the manufacture of the drug
Phenobarbital, Tablet, 97.2 mg (NDC 0603-5168-21)Discontinuation of the manufacture of the drug
Phenobarbital, Tablet, 97.2 mg (NDC 0603-5168-32)Discontinuation of the manufacture of the drug
Moxifloxacin Injection
Fresenius Kabi USA, LLC
Anti-Infective
2025-10-29
To Be Discontinued
First posted by the FDA
2025-10-29
Presentations affected
1
Manufacturer contact
888-386-1300
Moxifloxacin, Injection, 400mg per 250mL (NDC 63323-850-74)Discontinuation of the manufacture of the drug
Pramlintide Acetate Injection
AstraZeneca AB
Endocrinology/Metabolism
2025-10-27
To Be Discontinued
First posted by the FDA
2025-10-27
Presentations affected
2
Manufacturer contact
800-236-9933
SymlinPen® 120 , Injection, 1000 ug/1 mL (NDC 0310-6627-02)Discontinuation of the manufacture of the drug.
SymlinPen® 60 , Injection, 1000 ug/1 mL (NDC 0310-6615-02)Discontinuation of the manufacture of the drug.
Busulfan Injection
Mylan Institutional, a Viatris Company
Hematology
2025-10-24
To Be Discontinued
First posted by the FDA
2025-10-24
Presentations affected
1
Manufacturer contact
800-796-9526
Busulfan, Injection, 6 mg/1 mL (NDC 67457-893-08)Discontinuation of the manufacture of the drug.
Insulin Glargine Injection
Eli Lilly and Co.
Endocrinology/Metabolism
2025-10-24
To Be Discontinued
First posted by the FDA
2025-10-24
Presentations affected
1
Manufacturer contact
800-545-5979
Basaglar, Injection, U-100 Tempo Pen (NDC 0002-8214-05)A business decision was made to discontinue manufacture of the drug.
Insulin Lispro-aabc Injection
Eli Lilly and Co.
Endocrinology/Metabolism
2025-10-24
To Be Discontinued
First posted by the FDA
2025-10-24
Presentations affected
2
Manufacturer contact
800-545-5979
Lyumjev, Injection, U-100 Tempo Pen (NDC 0002-8235-05)A business decision was made to discontinue manufacture of the drug.
Lyumjev, Injection, U-100 Tempo Pen Sample (NDC 0002-8235-99)A business decision was made to discontinue manufacture of the drug.
Prazosin Hydrochloride Capsule
Pfizer Inc.
Cardiovascular
2023-04-28
To Be Discontinued
First posted by the FDA
2023-04-28
Presentations affected
3
Manufacturer contact
800-533-4535
Minipress, Capsule, 1 mg (NDC 0069-4310-71)Discontinuation of the manufacture of the drug. Supply expected to exhaust in August 2023
Minipress, Capsule, 2 mg (NDC 0069-4370-71)Discontinuation of the manufacture of the drug. Supply expected to exhaust in September 2023
Minipress, Capsule, 5 mg (NDC 0069-4380-71)Discontinuation of the manufacture of the drug. Supply expected to exhaust in September 2023
About
About the FDA drug shortage list
BuyandBill.com publishes the FDA's drug shortages on a daily basis. Our data comes directly
from the FDA's Drug Shortages Staff (DSS), the team responsible for tracking, preventing, and
helping to resolve shortages of medically necessary drugs.
The table covers three kinds of status: drugs currently in shortage, drugs whose shortage has
been resolved, and products that manufacturers have reported they intend to discontinue.
The process
How the FDA tracks and resolves a shortage
A shortage moves through a defined path, from the manufacturer's first notification to the FDA
confirming that supply has recovered.
Manufacturer notification
Under the FDA Safety and Innovation Act, manufacturers must notify the FDA of a permanent discontinuance or a temporary interruption in supply, generally at least six months in advance.
FDA assessment
The Drug Shortages Staff (DSS) evaluate the supply situation, confirm whether demand exceeds available supply, and add the affected product to the shortage list.
Mitigation
The FDA works with manufacturers to address the underlying cause, and may expedite review of related submissions or use regulatory flexibility to help restore supply.
Resolution
Once manufacturers confirm that supply can again meet demand, the DSS marks the shortage resolved and the listing is updated.
FAQ
Frequently asked questions
What is a drug shortage?
The FDA defines a drug shortage as a period when the demand or projected demand for a drug within the United States exceeds its supply.
Shortages can affect any drug, but they are especially disruptive for office-administered, buy-and-bill products that providers must keep on hand.
Where does BuyandBill.com's shortage data come from?
All of the data on this page is sourced from the FDA's Drug Shortages Staff (DSS), the team within the Center for Drug Evaluation and Research that tracks, prevents, and helps resolve shortages.
BuyandBill.com refreshes the list daily so the status of each product stays current.
What is the difference between a shortage and a discontinuation?
A shortage is a temporary gap between supply and demand that the FDA expects manufacturers to resolve.
A discontinuation is a manufacturer permanently removing a product from the market. Manufacturers are required to report planned discontinuances to the FDA in advance.
Why do drug shortages happen?
Common causes include manufacturing and product-quality problems, production delays, shortages of raw materials or active ingredients, business decisions to discontinue a product, and unexpected surges in demand.
How do shortages affect buy and bill?
When an office-administered drug is in shortage or discontinued, providers may have to substitute an alternative product. That substitution can change the NDC, the HCPCS code billed, and the resulting reimbursement.
Chart a whole drug class in one screen.
The Comparative Report puts ASP, the Medicare payment limit, WAC and AWP for up to
15 drugs on one timeline. Ten-plus years of monthly history, per HCPCS unit.
Four benchmarks plus the ASP/WAC ratio on the same axis
Prebuilt biosimilar, therapeutic-area and mechanism groups
Index to 100 to compare a $7 drug against a $90 one
Sortable table, reference multiples, saved reports, PDF export