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Glipizide

NDC 80425-0437 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAdvanced Rx of Tennessee, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA074497
Dosage form / routeTABLET · ORAL
Active ingredientsGLIPIZIDE (10 mg/1)
Marketing started20240903
Package count3

External sources

Source: openFDA. Public-domain (CC0).