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BRUKINSA

NDC 72579-122 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namezanubrutinib
Labeler / ManufacturerBeOne Medicines USA, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA218785
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsZANUBRUTINIB (160 mg/1)
Marketing started20250818
Package count1

External sources

Source: openFDA. Public-domain (CC0).