FDA NDC Directory · JSON-LD · Markdown

Finasteride

NDC 17856-0090 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namefinasteride
Labeler / ManufacturerAtlantic Biologicals Corps
Marketing categoryAbbreviated NDA (generic) · App ANDA090121
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFINASTERIDE (5 mg/1)
Marketing started20100528
Package count1

External sources

Source: openFDA. Public-domain (CC0).