FDA NDC Directory · JSON-LD · Markdown

PROPECIA

NDC 78206-152 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namefinasteride
Labeler / ManufacturerOrganon LLC
Marketing categoryNew Drug Application (innovator) · App NDA020788
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFINASTERIDE (1 mg/1)
Marketing started20210601
Package count2

External sources

Source: openFDA. Public-domain (CC0).