# Fenofibrate

NDC: 68180-388
Generic name: Fenofibrate
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200801

FDA application: ANDA090856

## Active ingredients

- FENOFIBRATE: 48 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68180-388"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68180-388
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=45364845-c3b4-40a1-a677-82202ffaa5ad