# Fenofibrate

NDC: 33342-340
Generic name: Fenofibrate
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20241113

FDA application: ANDA210248

## 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:"33342-340"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-340
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e8b9d1f5-0541-424f-b1d4-bef6381aa934