FDA NDC Directory · JSON-LD · Markdown

Metformin Hydrochloride

NDC 51655-644 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA209882
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (1000 mg/1)
Marketing started20230706
Package count1

External sources

Source: openFDA. Public-domain (CC0).