# Glimepiride

NDC: 71921-216
Generic name: Glimepiride
Labeler / Manufacturer: Florida Pharmaceutical Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230731

FDA application: ANDA202112

## 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:"71921-216"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71921-216
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8ff0de99-272e-4e68-9caf-69f3f146ac29