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Glimepiride

NDC 55111-322 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDr. Reddy's Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA077091
Dosage form / routeTABLET · ORAL
Active ingredientsGLIMEPIRIDE (4 mg/1)
Marketing started20051006
Package count4

External sources

Source: openFDA. Public-domain (CC0).