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Pazopanib

NDC 0480-4184 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerTeva Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217517
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsPAZOPANIB HYDROCHLORIDE (200 mg/1)
Marketing started20231020
Package count1

External sources

Source: openFDA. Public-domain (CC0).