# Fenofibrate

NDC: 71205-949
Generic name: Fenofibrate
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200423

FDA application: ANDA207803

## Active ingredients

- FENOFIBRATE: 160 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-949"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-949
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=41f0f514-1fa9-47a0-a085-a31354842f96