# Icosapent Ethyl

NDC: 0480-0127
Generic name: Icosapent Ethyl
Labeler / Manufacturer: Teva Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20221215

FDA application: ANDA209525

## 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:"0480-0127"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0480-0127
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de7049ae-d1d6-4267-a93b-dd5039c50c2c