# Gemfibrozil

NDC: 76282-225
Generic name: Gemfibrozil
Labeler / Manufacturer: Exelan Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20061020

FDA application: ANDA077836

## Active ingredients

- GEMFIBROZIL: 600 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"76282-225"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76282-225
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5c09fe54-697e-4cd5-9a26-7c9c7fa9a864