FDA NDC Directory · JSON-LD · Markdown

Finasteride

NDC 68788-6875 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203687
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFINASTERIDE (1 mg/1)
Marketing started20170123
Package count3

External sources

Source: openFDA. Public-domain (CC0).