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Abiraterone acetate

NDC 71921-177 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerFlorida Pharmaceutical Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA215086
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsABIRATERONE ACETATE (500 mg/1)
Marketing started20230410
Package count1

External sources

Source: openFDA. Public-domain (CC0).