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Abiraterone Acetate

NDC 0378-6921 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameabiraterone acetate
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208446
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsABIRATERONE ACETATE (500 mg/1)
Marketing started20201214
Package count1

External sources

Source: openFDA. Public-domain (CC0).