FDA NDC Directory · JSON-LD · Markdown

Finasteride

NDC 70518-2287 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA207750
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsFINASTERIDE (1 mg/1)
Marketing started20190827
Package count2

External sources

Source: openFDA. Public-domain (CC0).