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  5. NDC Package Code: 66215-402-01 Veletri

NDC Package 66215-402-01 Veletri

Epoprostenol Injection, Powder, Lyophilized, For Solution Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
66215-402-01
Package Description:
1 VIAL in 1 CARTON / 10 mL in 1 VIAL
Product Code:
66215-402
Proprietary Name:
Veletri
Non-Proprietary Name:
Epoprostenol
Substance Name:
Epoprostenol
Usage Information:
This medication is used to treat high blood pressure in the lungs (pulmonary arterial hypertension). It helps to increase your ability to exercise and improve symptoms such as shortness of breath and tiredness. It works by relaxing and widening the blood vessels (arteries) in the lungs and other parts of the body so that blood can flow more easily. This medication belongs to a class of drugs known as vasodilators.
11-Digit NDC Billing Format:
66215040201
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1009216 - VELETRI 1.5 MG Injection
  • RxCUI: 1009216 - epoprostenol 1.5 MG Injection [Veletri]
  • RxCUI: 1009216 - Veletri 1.5 MG (as epoprostenol sodium) Injection
  • RxCUI: 1302755 - VELETRI 0.5 MG Injection
  • RxCUI: 1302755 - epoprostenol 0.5 MG Injection [Veletri]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Actelion Pharmaceuticals Us, Inc.
    Dosage Form:
    Injection, Powder, Lyophilized, For Solution - A dosage form intended for the solution prepared by lyophilization ("freeze drying"), a process which involves the removal of water from products in the frozen state at extremely low pressures; this is intended for subsequent addition of liquid to create a solution that conforms in all respects to the requirements for Injections.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • EPOPROSTENOL 1.5 mg/10mL
    • Pharmacologic Class(es):
  • Prostacycline Vasodilator - [EPC] (Established Pharmacologic Class)
  • Prostaglandins I - [CS]
  • Vasodilation - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    NDA022260
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    04-22-2010
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 66215-402-01 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    66215040201J1325Epoprostenol injection0.5 MG1133

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 66215-402-01?

    The NDC Packaged Code 66215-402-01 is assigned to a package of 1 vial in 1 carton / 10 ml in 1 vial of Veletri, a human prescription drug labeled by Actelion Pharmaceuticals Us, Inc.. The product's dosage form is injection, powder, lyophilized, for solution and is administered via intravenous form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

    Is NDC 66215-402 included in the NDC Directory?

    Yes, Veletri with product code 66215-402 is active and included in the NDC Directory. The product was first marketed by Actelion Pharmaceuticals Us, Inc. on April 22, 2010 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 66215-402-01?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 66215-402-01?

    The 11-digit format is 66215040201. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-266215-402-015-4-266215-0402-01