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febuxostat

NDC 70771-1553 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Lifesciences Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA205443
Dosage form / routeTABLET · ORAL
Active ingredientsFEBUXOSTAT (80 mg/1)
Marketing started20230331
Package count6

External sources

Source: openFDA. Public-domain (CC0).