NDC codes

FDA NDC Directory
Product NDC (as listed)55150-219Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55150-0219Add 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
55150-219-1055150021910551500219101 VIAL, SINGLE-DOSE in 1 CARTON (55150-219-10) / 10 mL in 1 VIAL, SINGLE-DOSEMarketed from Dec 8, 2015

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)
Eptifibatide
Generic name (nonproprietary)
eptifibatide
Active ingredients
Eptifibatide — 20 mg/10mL
Dosage form
Injection
Route
Intravenous
Labeler
Eugia US LLCNDC labeler code 55150
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 206127
Marketing start
Listing expires
Other FDA classes
Decreased Platelet Aggregation (Physiologic effect)
Identifiers
Product ID 55150-219_944b269c-d810-411d-9ed4-8edd9d0ac1b7SPL ID 944b269c-d810-411d-9ed4-8edd9d0ac1b7SPL set ID 00ad7bbe-cadd-4647-b74b-adfc9f2b5e94RxCUI 200349, 1736470, 1736477UNII NA8320J834UPC 0355150220991, 0355150219100
Pharmacologic class
Platelet Aggregation Inhibitor

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N455150021910 followed by a unit qualifier and the quantity

Package 55150-0219-10. 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)

Eptifibatide injection is a platelet aggregation inhibitor indicated for: Treatment of acute coronary syndrome (ACS) managed medically or with percutaneous coronary intervention (PCI) (1.1) Treatment of patients undergoing PCI (including intracoronary stenting) (1.2) 1.1 Acute Coronary Syndrome (ACS) Eptifibatide injection is indicated to decrease the rate of a combined endpoint of death or new myocardial infarction (MI) in patients with ACS (unstable angina [UA]/non-ST-elevation myocardial infarction [NSTEMI]), including patients who are to be managed medically and those undergoing percutaneous coronary intervention (PCI). 1.2 Percutaneous Coronary Intervention (PCI) Eptifibatide injection …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 55150-219

What is NDC 55150-219?
55150-219 is the product NDC for Eptifibatide, Eptifibatide 20 mg/10mL injection, listed with the FDA by Eugia US LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Eptifibatide.
What is the active ingredient?
Eptifibatide.
Who is the labeler?
Eugia US LLC, NDC labeler code 55150. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Eptifibatide?
20 other product NDCs are listed under this name. See all Eptifibatide NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Eptifibatide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
EptifibatideEptifibatide 2 mg/mLInjection, SolutionIntravenousMeitheal Pharmaceuticals Inc.71288-41271288-0412-10
EptifibatideEptifibatide .75 mg/mLInjection, SolutionIntravenousMeitheal Pharmaceuticals Inc.71288-41371288-0413-51
EptifibatideEptifibatide 2 mg/mLInjection, SolutionIntravenousAvenacy, LLC83634-30083634-0300-10
EptifibatideEptifibatide .75 mg/mLInjection, SolutionIntravenousAvenacy, LLC83634-30183634-0301-51
EptifibatideEptifibatide .75 mg/mLInjection, SolutionIntravenousHainan Shuangcheng Pharmaceuticals Co., Ltd.52958-04052958-0040-01
EptifibatideEptifibatide 2 mg/mLInjection, SolutionIntravenousHainan Shuangcheng Pharmaceuticals Co., Ltd.52958-40252958-0402-01
EptifibatideEptifibatide 2 mg/mLInjection, SolutionIntravenousMylan Institutional LLC72078-02572078-0025-10
EptifibatideEptifibatide 2 mg/mLInjection, SolutionIntravenousMylan Institutional LLC72078-02772078-0027-10
EptifibatideEptifibatide .75 mg/mLInjection, SolutionIntravenousMylan Institutional LLC72078-02672078-0026-10
EptifibatideEptifibatide 2 mg/mLInjectionIntravenousSlate Run Pharmaceuticals, LLC70436-02670436-0026-80

All 21 Eptifibatide NDCs

Other NDCs under ANDA 206127

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

FDA NDC Directory listings under ANDA 206127
ProductStrengthForm · routeLabelerProduct NDC
EptifibatideEptifibatide 75 mg/100mLInjectionIntravenousEugia US LLC55150-218
EptifibatideEptifibatide 200 mg/100mLInjectionIntravenousEugia US LLC55150-220

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