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glyburide

NDC 68382-656 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerZydus Pharmaceuticals (USA) Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA206749
Dosage form / routeTABLET · ORAL
Active ingredientsGLYBURIDE (1.25 mg/1)
Marketing started20160602
Package count6

External sources

Source: openFDA. Public-domain (CC0).