# Glimepiride

NDC: 42571-101
Generic name: Glimepiride
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20130613

FDA application: ANDA091220

## Active ingredients

- GLIMEPIRIDE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42571-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=60e9397e-83b9-489e-9683-6f87e458bbaa