# GEMFIBROZIL

NDC: 68788-7964
Generic name: Gemfibrozil
Labeler / Manufacturer: Preferred Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20210720

FDA application: ANDA214603

## 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:"68788-7964"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-7964
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2f5738ac-1c9c-4f3a-8c7d-6039d768831e