FDA NDC Directory · JSON-LD · Markdown

METFORMIN HYDROCHLORIDE

NDC 68462-520 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic namemetformin hydrochloride
Labeler / ManufacturerGLENMARK PHARMACEUTICALS INC., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA212969
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsMETFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20191125
Package count3

External sources

Source: openFDA. Public-domain (CC0).