# ICOSAPENT ETHYL

NDC: 42806-560
Generic name: icosapent ethyl
Labeler / Manufacturer: EPIC PHARMA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20231222

FDA application: ANDA217919

## Active ingredients

- ICOSAPENT ETHYL: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42806-560"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-560
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6db749b9-c817-41cd-909f-dd60a90c9f73