# Gemfibrozil

NDC: 75834-131
Generic name: Gemfibrozil
Labeler / Manufacturer: Nivagen Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170215

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:"75834-131"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=75834-131
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a086fc16-e6f3-47fd-b577-7c611e735834