# Gemfibrozil

NDC: 68382-553
Generic name: Gemfibrozil
Labeler / Manufacturer: Zydus Pharmaceuticals (USA) Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190115

FDA application: ANDA204189

## Active ingredients

- GEMFIBROZIL: 600 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68382-553"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68382-553
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=556945e8-4100-4538-bcba-af5b2f13a7e8