FDA NDC Directory · JSON-LD · Markdown

Finasteride

NDC 71335-0433 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namefinasteride
Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA090121
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFINASTERIDE (5 mg/1)
Marketing started20100528
Package count6

External sources

Source: openFDA. Public-domain (CC0).