Amgen
KANJINTI
Manufacturer:
Amgen
Name:
KANJINTI
HCPCS Code Descriptor:
Injection, trastuzumab-anns, biosimilar, (kanjinti), 10 mg
Category:
Q Code
HCPCS:
Q5117
NDC(s):
55513-0164-01, 55513-0132-01, 55513-0141-01
Primary Type:
Oncology Biosimilar
Generic Status:
Single-Source
Route of Administration:
Intravenous
About:
KANJINTI is an Oncology Biosimilar drug manufactured by Amgen and administered via the Intravenous route of administration. The Q Code: Q5117 is aligned to the drug KANJINTI.
Kanjinti (trastuzumab) is a HER2 inhibitor that is used to treat certain types of stomach and breast cancer. Kanjinti can be used by itself or in combination with other cancer medications. It is manufactured by Amgen USA and is biosimilar to the medication Herceptin (J9356). Kanjinti has been aligned to the Q Code Q5117 since October 2019.
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HCPCS Added Date:
10/1/19
HCPCS Effective Date:
10/1/19
HCPCS Short Description:
Inj., kanjinti, 10 mg
Billing and Coding Guide:
https://www.kanjinti.com/-/media/Themes/Amgen/Kanjinti/Kanjinti/docs/Kanjinti-Billing-and-Coding-Guide.pdf
Patient Assistance:
Not Found