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Glimepiride

NDC 70518-4774 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA202112
Dosage form / routeTABLET · ORAL
Active ingredientsGLIMEPIRIDE (1 mg/1)
Marketing started20261015
Package count1

External sources

Source: openFDA. Public-domain (CC0).