FDA NDC Directory · JSON-LD · Markdown

Metformin Hydrochloride

NDC 69367-381 · HUMAN PRESCRIPTION DRUG · TABLET, COATED

Labeler / ManufacturerWestminster Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205096
Dosage form / routeTABLET, COATED · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20240304
Package count3

External sources

Source: openFDA. Public-domain (CC0).