# Fenofibrate

NDC: 0378-3066
Generic name: fenofibrate
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20130514

FDA application: ANDA202856

## Active ingredients

- FENOFIBRATE: 145 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0378-3066"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-3066
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0f958942-1504-40a1-8ad8-43df2c3f717e