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Glipizide

NDC 68788-4178 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074378
Dosage form / routeTABLET · ORAL
Active ingredientsGLIPIZIDE (5 mg/1)
Marketing started20260731
Package count5

External sources

Source: openFDA. Public-domain (CC0).