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Glipizide

NDC 68071-4232 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075795
Dosage form / routeTABLET · ORAL
Active ingredientsGLIPIZIDE (10 mg/1)
Marketing started20020925
Package count1

External sources

Source: openFDA. Public-domain (CC0).