FDA NDC Directory · JSON-LD · Markdown

PROSCAR

NDC 78206-153 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameFINASTERIDE
Labeler / ManufacturerOrganon LLC
Marketing categoryNew Drug Application (innovator) · App NDA020180
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsFINASTERIDE (5 mg/1)
Marketing started20210601
Package count2

External sources

Source: openFDA. Public-domain (CC0).