NDC codes

FDA NDC Directory
Product NDC (as listed)71335-3072Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71335-3072Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
71335-3072-17133530720130 CAPSULE in 1 BOTTLE (71335-3072-1)Marketed from Feb 9, 2026
71335-3072-27133530720260 CAPSULE in 1 BOTTLE (71335-3072-2)Marketed from Feb 9, 2026
71335-3072-371335307203120 CAPSULE in 1 BOTTLE (71335-3072-3)Marketed from Feb 9, 2026
71335-3072-47133530720490 CAPSULE in 1 BOTTLE (71335-3072-4)Marketed from Feb 9, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Icosapent Ethyl
Generic name (nonproprietary)
icosapent ethyl
Active ingredients
Icosapent ethyl — 1 g/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209457
Marketing start
Listing expires
Identifiers
Product ID 71335-3072_d96d5cdc-9abb-4546-aa0c-b5834d82478cSPL ID d96d5cdc-9abb-4546-aa0c-b5834d82478cSPL set ID 07631e74-48e5-46ec-b8db-4b1bcf62d283RxCUI 1304979UNII 6GC8A4PAYH

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N471335307201 followed by a unit qualifier and the quantity

Package 71335-3072-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Icosapent ethyl is indicated: • as an adjunct to diet to reduce triglyceride (TG) levels in adult patients with severe (≥500 mg/dL) hypertriglyceridemia. Limitations of Use The effect of icosapent ethyl on the risk for pancreatitis in patients with severe hypertriglyceridemia has not been determined. Icosapent ethyl capsules are an ethyl ester of eicosapentaenoic acid (EPA) indicated: • as an adjunct to diet to reduce triglyceride (TG) levels in adult patients with severe (≥ 500 mg/dL) hypertriglyceridemia. ( 1 ) Limitations of Use: • The effect of icosapent ethyl on the risk for pancreatitis in patients with severe hypertriglyceridemia has not been determined. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 209457

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 209457
ProductStrengthForm · routeLabelerProduct NDC
Icosapent EthylIcosapent ethyl 1 g/1CapsuleOralBryant Ranch Prepack71335-2842
Icosapent EthylIcosapent ethyl .5 g/1CapsuleOralHikma Pharmaceuticals USA Inc.0054-0621
Icosapent EthylIcosapent ethyl 1 g/1CapsuleOralHikma Pharmaceuticals USA Inc.0054-0508
Icosapent EthylIcosapent ethyl 1 g/1CapsuleOralBryant Ranch Prepack72162-1000
Icosapent EthylIcosapent ethyl 1 g/1CapsuleOralNorthstar Rx LLC72603-129
Icosapent EthylIcosapent ethyl 1 g/1CapsuleOralBryant Ranch Prepack63629-9311

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