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Glipizide

NDC 70518-1063 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA204720
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsGLIPIZIDE (5 mg/1)
Marketing started20180313
Package count2

External sources

Source: openFDA. Public-domain (CC0).