# Gemfibrozil

NDC: 71209-008
Generic name: Gemfibrozil
Labeler / Manufacturer: Cadila Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20160617

FDA application: ANDA203266

## Active ingredients

- GEMFIBROZIL: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71209-008"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71209-008
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0b50849a-66b6-4e8f-9f45-5425a875d366