FDA NDC Directory · JSON-LD · Markdown

Finasteride

NDC 57237-062 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078341
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFINASTERIDE (5 mg/1)
Marketing started20071030
Package count3

External sources

Source: openFDA. Public-domain (CC0).