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Glyburide

NDC 66267-103 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090937
Dosage form / routeTABLET · ORAL
Active ingredientsGLYBURIDE (5 mg/1)
Marketing started20101005
Package count4

External sources

Source: openFDA. Public-domain (CC0).