United States · FDA National Drug Code directory
Icosapent Ethyl
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 67184-0582_324fd508-befc-404a-8f75-97b35d2df694
- Product NDC
- 67184-0582
- Form
- CAPSULE
- Composition / generic term
- Icosapent Ethyl
- Labeler
- Qilu Pharmaceutical Co., Ltd.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250101
- Source listing expiry
- 20261231
Source-listed ingredients
- ICOSAPENT ETHYL — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 120 CAPSULE in 1 BOTTLE (67184-0582-1) · 67184-0582-1
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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