RecallHawk

KANJINTI (TRASTUZUMAB-ANNS)

AMGEN INC

Summary

FDA approved KANJINTI (TRASTUZUMAB-ANNS) by AMGEN INC. BLA (Biologic) approval on 2024-12-19. VIAL, SINGLE-DOSE.

Details

Source

Drug Approval

External ID

BLA761073-10

Action Date

2024-12-19

Status

Approved

Category

drug

Product Code

BLA (Biologic)

Product Description

KANJINTI (generic: TRASTUZUMAB-ANNS), VIAL, SINGLE-DOSE. Application: BLA761073

Company

Context & Analysis

AMGEN INC has 9 FDA actions in our database, including 3 recalls.

Frequently Asked Questions

How often does AMGEN INC have FDA actions?

AMGEN INC has 9 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "BLA761073-10" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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