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Glimepiride

NDC 42571-101 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA091220
Dosage form / routeTABLET · ORAL
Active ingredientsGLIMEPIRIDE (2 mg/1)
Marketing started20130613
Package count2

External sources

Source: openFDA. Public-domain (CC0).