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Glimepiride

NDC 43063-587 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPD-Rx Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA078181
Dosage form / routeTABLET · ORAL
Active ingredientsGLIMEPIRIDE (4 mg/1)
Marketing started20070823
Package count2

External sources

Source: openFDA. Public-domain (CC0).