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
- 71335-3148_4d05c006-9a8b-4b54-b835-3ab2810e1dc1
- Product NDC
- 71335-3148
- Form
- CAPSULE, LIQUID FILLED
- Composition / generic term
- icosapent ethyl
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20231222
- Source listing expiry
- 20271231
Source-listed ingredients
- ICOSAPENT ETHYL — 1 g/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3148-1) · 71335-3148-1
- 60 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3148-2) · 71335-3148-2
- 120 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3148-3) · 71335-3148-3
- 90 CAPSULE, LIQUID FILLED in 1 BOTTLE (71335-3148-4) · 71335-3148-4
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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