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Febuxostat

NDC 0904-7484 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA210461
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFEBUXOSTAT (40 mg/1)
Marketing started20240522
Marketing ended20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).