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  5. NDC Package Code: 66302-302-10 Orenitram

NDC Package 66302-302-10 Orenitram

Treprostinil Tablet, Extended Release Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    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:
66302-302-10
Package Description:
10 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Code:
66302-302
Proprietary Name:
Orenitram
Non-Proprietary Name:
Treprostinil
Substance Name:
Treprostinil
Usage Information:
This medication is used to treat a type of high blood pressure in the lungs (pulmonary arterial hypertension). Treprostinil helps to increase your ability to exercise and improves 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:
66302030210
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
10 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 1488665 - treprostinil 0.125 MG 12HR Extended Release Oral Tablet
  • RxCUI: 1488665 - 12 HR treprostinil 0.125 MG Extended Release Oral Tablet
  • RxCUI: 1488665 - treprostinil 0.125 MG (as treprostinil diethanolamine) 12 HR Extended Release Oral Tablet
  • RxCUI: 1488665 - treprostinil 0.125 MG (as treprostinil diolamine 0.159 MG) 12 HR Extended Release Oral Tablet
  • RxCUI: 1488667 - Orenitram 0.125 MG 12HR Extended Release Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    United Therapeutics Corporation
    Dosage Form:
    Tablet, Extended Release - A solid dosage form containing a drug which allows at least a reduction in dosing frequency as compared to that drug presented in conventional dosage form.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • TREPROSTINIL .25 mg/1
    • Pharmacologic Class(es):
  • Prostacycline Vasodilator - [EPC] (Established Pharmacologic Class)
  • Prostaglandins I - [CS]
  • Vasodilation - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    NDA203496
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    12-20-2013
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    66302-302-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE
    66302-302-021 BLISTER PACK in 1 CARTON / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 66302-302-10?

    The NDC Packaged Code 66302-302-10 is assigned to a package of 10 tablet, extended release in 1 bottle of Orenitram, a human prescription drug labeled by United Therapeutics Corporation. The product's dosage form is tablet, extended release and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 10 billable units per package.

    Is NDC 66302-302 included in the NDC Directory?

    Yes, Orenitram with product code 66302-302 is active and included in the NDC Directory. The product was first marketed by United Therapeutics Corporation on December 20, 2013 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 66302-302-10?

    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 10.

    What is the 11-digit format for NDC 66302-302-10?

    The 11-digit format is 66302030210. 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
    5-3-266302-302-105-4-266302-0302-10