# Fenofibrate

NDC: 48433-040
Generic name: fenofibrate
Labeler / Manufacturer: Safecor Health, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260317

FDA application: ANDA202856

## Active ingredients

- FENOFIBRATE: 145 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"48433-040"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=48433-040
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9cc2038d-750e-42dc-b818-c5642cf6a5ad