NDC Package 66215-628-20 Uptravi Titration Pack

Selexipag Kit - View Billable Units, 11-Digit Format, RxNorm

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:
66215-628-20
Package Description:
1 KIT in 1 CARTON * 1 BOTTLE in 1 CARTON / 140 TABLET, COATED in 1 BOTTLE * 1 BOTTLE in 1 CARTON / 60 TABLET, COATED in 1 BOTTLE
Product Code:
Proprietary Name:
Uptravi Titration Pack
Non-Proprietary Name:
Selexipag
Usage Information:
Selexipag is used to treat high blood pressure in the lungs (pulmonary arterial hypertension-PAH). It is used to help slow down worsening of PAH and to decrease the chance of needing treatment in a hospital. Selexipag works by making it easier for blood to flow through the arteries in your lungs. This effect helps increase your ability to exercise.
11-Digit NDC Billing Format:
66215062820
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 1729007 - selexipag 1000 MCG Oral Tablet
  • RxCUI: 1729007 - selexipag 1 MG Oral Tablet
  • RxCUI: 1729013 - Uptravi 1000 MCG Oral Tablet
  • RxCUI: 1729013 - selexipag 1 MG Oral Tablet [Uptravi]
  • RxCUI: 1729013 - Uptravi 1 MG Oral Tablet
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Actelion Pharmaceuticals Us, Inc.
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    NDA207947
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    12-21-2015
    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.

    Frequently Asked Questions

    What is NDC 66215-628-20?

    The NDC Packaged Code 66215-628-20 is assigned to a package of 1 kit in 1 carton * 1 bottle in 1 carton / 140 tablet, coated in 1 bottle * 1 bottle in 1 carton / 60 tablet, coated in 1 bottle of Uptravi Titration Pack, a human prescription drug labeled by Actelion Pharmaceuticals Us, Inc.. The product's dosage form is kit and is administered via form.

    Is NDC 66215-628 included in the NDC Directory?

    Yes, Uptravi Titration Pack with product code 66215-628 is active and included in the NDC Directory. The product was first marketed by Actelion Pharmaceuticals Us, Inc. on December 21, 2015 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 66215-628-20?

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

    What is the 11-digit format for NDC 66215-628-20?

    The 11-digit format is 66215062820. 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
    5-3-266215-628-205-4-266215-0628-20