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Glipizide

NDC 68788-0141 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA075795
Dosage form / routeTABLET · ORAL
Active ingredientsGLIPIZIDE (5 mg/1)
Marketing started20130218
Package count4

External sources

Source: openFDA. Public-domain (CC0).