Amgen

KANJINTI

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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.

Access Pricing and More By Registering

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