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Abiraterone

NDC 72205-285 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameAbiraterone acetate
Labeler / ManufacturerNovadoz Pharmaceuticals LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA210686
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsABIRATERONE ACETATE (500 mg/1)
Marketing started20240424
Package count2

External sources

Source: openFDA. Public-domain (CC0).