# Fenofibrate

NDC: 31722-596
Generic name: Fenofibrate
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160714

FDA application: ANDA204598

## Active ingredients

- FENOFIBRATE: 145 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-596"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-596
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=38f43148-4ca0-402a-ba39-8ee5011a7907