FDA NDC Directory · JSON-LD · Markdown

METFORMIN HYDROCHLORIDE

NDC 82009-175 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerQuallent Pharmaceuticals Health LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA203686
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (1000 mg/1)
Marketing started20250718
Package count1

External sources

Source: openFDA. Public-domain (CC0).