# Gemfibrozil

NDC: 72603-206
Generic name: Gemfibrozil
Labeler / Manufacturer: NorthStar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150916

FDA application: ANDA202726

## 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:"72603-206"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-206
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b5e33ee2-f766-41d6-8a4b-7b4f0e961bf4