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Abiraterone Acetate

NDC 82293-002 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameabiraterone acetate
Labeler / ManufacturerNovugen Pharma (USA) LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215947
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsABIRATERONE ACETATE (500 mg/1)
Marketing started20220105
Package count1

External sources

Source: openFDA. Public-domain (CC0).