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Glimepiride

NDC 43547-396 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameglimepiride
Labeler / ManufacturerSolco Healthcare U.S., LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA077370
Dosage form / routeTABLET · ORAL
Active ingredientsGLIMEPIRIDE (4 mg/1)
Marketing started20170130
Package count2

External sources

Source: openFDA. Public-domain (CC0).