# fenofibrate

NDC: 68462-582
Generic name: fenofibrate
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20170407

FDA application: ANDA205566

## Active ingredients

- FENOFIBRATE: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68462-582"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-582
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e7204052-02cf-4b38-835b-d8754c74b2cd