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Glipizide

NDC 68788-8487 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204720
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsGLIPIZIDE (2.5 mg/1)
Marketing started20230719
Package count4

External sources

Source: openFDA. Public-domain (CC0).