# fenofibrate

NDC: 42385-950
Generic name: fenofibrate
Labeler / Manufacturer: Laurus Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200318

FDA application: ANDA211122

## Active ingredients

- FENOFIBRATE: 48 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42385-950"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42385-950
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0da6d56e-1ed6-437d-b88d-16b014d1889a