# Gemfibrozil

NDC: 16571-784
Generic name: Gemfibrozil
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
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:"16571-784"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16571-784
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8f36abfa-dc52-4c99-8a4a-b0cb80c3249a