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Glimepiride

NDC 51655-120 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA078181
Dosage form / routeTABLET · ORAL
Active ingredientsGLIMEPIRIDE (4 mg/1)
Marketing started20141229
Package count2

External sources

Source: openFDA. Public-domain (CC0).