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Glyburide

NDC 71209-010 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerCadila Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA203379
Dosage form / routeTABLET · ORAL
Active ingredientsGLYBURIDE (2.5 mg/1)
Marketing started20140426
Package count3

External sources

Source: openFDA. Public-domain (CC0).