FDA NDC Directory · JSON-LD · Markdown

Finasteride

NDC 0904-6830 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA090061
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFINASTERIDE (5 mg/1)
Marketing started20150613
Package count2

External sources

Source: openFDA. Public-domain (CC0).