NDC Package 66302-150-50 Sterile Diluent For Remodulin

Water Injection, Solution Intravenous - 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:
66302-150-50
Package Description:
1 VIAL in 1 BOX / 50 mL in 1 VIAL
Product Code:
Proprietary Name:
Sterile Diluent For Remodulin
Non-Proprietary Name:
Water
Substance Name:
Water
Usage Information:
None
11-Digit NDC Billing Format:
66302015050
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 2590175 - treprostinil 20 MG/ML Injectable Solution
  • RxCUI: 2590177 - Remodulin 20 MG/ML Injectable Solution
  • RxCUI: 2590177 - treprostinil 20 MG/ML Injectable Solution [Remodulin]
  • RxCUI: 2667748 - treprostinil 0.1 MG/ML Injectable Solution
  • RxCUI: 2667750 - Remodulin 0.1 MG/ML Injectable Solution
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    United Therapeutics Corporation
    Dosage Form:
    Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA021272
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    05-22-2002
    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 66302-150-50?

    The NDC Packaged Code 66302-150-50 is assigned to a package of 1 vial in 1 box / 50 ml in 1 vial of Sterile Diluent For Remodulin, a human prescription drug labeled by United Therapeutics Corporation. The product's dosage form is injection, solution and is administered via intravenous form.

    Is NDC 66302-150 included in the NDC Directory?

    Yes, Sterile Diluent For Remodulin with product code 66302-150 is active and included in the NDC Directory. The product was first marketed by United Therapeutics Corporation on May 22, 2002 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 66302-150-50?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 66302-150-50?

    The 11-digit format is 66302015050. 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
    5-3-266302-150-505-4-266302-0150-50