FDA NDC Directory · JSON-LD · Markdown

Glyburide and Metformin Hydrochloride

NDC 68788-7180 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA077870
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsGLYBURIDE (2.5 mg/1)
METFORMIN HYDROCHLORIDE (500 mg/1)
Marketing started20180716
Package count4

External sources

Source: openFDA. Public-domain (CC0).