FDA NDC Directory · JSON-LD · Markdown

Finasteride

NDC 67877-288 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA204304
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFINASTERIDE (5 mg/1)
Marketing started20170105
Package count6

External sources

Source: openFDA. Public-domain (CC0).