FDA NDC Directory · JSON-LD · Markdown

Glyburide

NDC 71209-009 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCadila Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203379
Dosage form / routeTABLET · ORAL
Active ingredientsGLYBURIDE (1.25 mg/1)
Marketing started20140426
Package count2

External sources

Source: openFDA. Public-domain (CC0).