FDA NDC Directory · JSON-LD · Markdown

Finasteride

NDC 65862-149 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078341
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFINASTERIDE (5 mg/1)
Marketing started20071030
Package count4

External sources

Source: openFDA. Public-domain (CC0).