# Glimepiride

NDC: 55111-322
Generic name: Glimepiride
Labeler / Manufacturer: Dr. Reddy's Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20051006

FDA application: ANDA077091

## Active ingredients

- GLIMEPIRIDE: 4 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55111-322"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-322
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=07ad4366-4b21-f633-49f3-c2b35f88168d