FDA NDC Directory · JSON-LD · Markdown

Abiraterone

NDC 0143-9597 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameAbiraterone acetate
Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208339
Dosage form / routeTABLET · ORAL
Active ingredientsABIRATERONE ACETATE (250 mg/1)
Marketing started20181123
Package count1

External sources

Source: openFDA. Public-domain (CC0).