FDA NDC Directory · JSON-LD · Markdown

Abiraterone Acetate

NDC 0378-6920 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameabiraterone acetate
Labeler / ManufacturerMylan Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA208446
Dosage form / routeTABLET · ORAL
Active ingredientsABIRATERONE ACETATE (250 mg/1)
Marketing started20181121
Package count1

External sources

Source: openFDA. Public-domain (CC0).