# FENOFIBRATE

NDC: 82619-101
Generic name: fenofibrate
Labeler / Manufacturer: Creekwood Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230907

FDA application: ANDA217732

## Active ingredients

- FENOFIBRATE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82619-101"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82619-101
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=65d8aefc-7ec2-4f62-9254-5f0070c58ac2