NDC codes

FDA NDC Directory
Product NDC (as listed)52937-005Labeler and product segments. Claims need a package NDC.
Product NDC at billing width52937-0005Add 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
52937-005-2052937000520120 CAPSULE in 1 BOTTLE (52937-005-20)Marketed from Dec 5, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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)
Vascepa
Generic name (nonproprietary)
icosapent ethyl
Active ingredients
Icosapent ethyl1000 mg/1
Dosage form
Capsule
Route
Oral
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 202057
Marketing start
Listing expires
Identifiers
Product ID 52937-005_86b35fe3-d1cf-478e-849b-2ea0c87bda33SPL ID 86b35fe3-d1cf-478e-849b-2ea0c87bda33SPL set ID 9c1a2828-1583-4414-ab22-a60480e8e508RxCUI 1304979, 1304985, 1811180, 1811182UNII 6GC8A4PAYHUPC 0352937001200

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

N452937000520 followed by a unit qualifier and the quantity

Package 52937-0005-20. 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)

VASCEPA ® (icosapent ethyl) is indicated: as an adjunct to maximally tolerated statin therapy to reduce the risk of myocardial infarction, stroke, coronary revascularization, and unstable angina requiring hospitalization in adult patients with elevated triglyceride (TG) levels (≥ 150 mg/dL) and established cardiovascular disease or diabetes mellitus and 2 or more additional risk factors for cardiovascular disease. as an adjunct to diet to reduce TG levels in adult patients with severe (≥ 500 mg/dL) hypertriglyceridemia. Limitations of Use: The effect of VASCEPA on the risk for pancreatitis in patients with severe hypertriglyceridemia has not been determined. VASCEPA is an ethyl ester of eico

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 202057

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

FDA NDC Directory listings under NDA 202057
ProductStrengthForm · routeLabelerProduct NDC
Vascepaicosapent ethylIcosapent ethyl 1000 mg/1CapsuleOralAmarin Pharma Inc.52937-001
Vascepaicosapent ethylIcosapent ethyl 500 mg/1CapsuleOralAmarin Pharma Inc.52937-003
Vascepaicosapent ethylIcosapent ethyl 1000 mg/1CapsuleOralAmarin Pharma Inc.52937-101
Vascepaicosapent ethylIcosapent ethyl 1000 mg/1CapsuleOralBryant Ranch Prepack63629-8247

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