FDA NDC Directory · JSON-LD · Markdown

Abiraterone Acetate

NDC 75907-224 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDr. Reddys Laboratories Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA208416
Dosage form / routeTABLET · ORAL
Active ingredientsABIRATERONE ACETATE (250 mg/1)
Marketing started20250317
Package count1

External sources

Source: openFDA. Public-domain (CC0).