# FENOFIBRATE

NDC: 50268-313
Generic name: FENOFIBRATE
Labeler / Manufacturer: AvPAK
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20150813

FDA application: ANDA076509

## Active ingredients

- FENOFIBRATE: 160 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50268-313"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50268-313
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d4e1d692-3c03-7406-ee06-7a6fb39ed3e7