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Glipizide

NDC 59651-782 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206928
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsGLIPIZIDE (10 mg/1)
Marketing started20230303
Package count4

External sources

Source: openFDA. Public-domain (CC0).