# FENOFIBRATE

NDC: 42385-935
Generic name: FENOFIBRATE
Labeler / Manufacturer: Laurus Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200113

FDA application: ANDA210606

## Active ingredients

- FENOFIBRATE: 54 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42385-935"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42385-935
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8e58c13a-8088-4fed-86cc-52530de5aa45