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  5. NDC Package Code: 72189-002-25 Albuterol Sulfate

NDC Package 72189-002-25 Albuterol Sulfate

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
72189-002-25
Package Description:
3 mL in 1 BOTTLE
Product Code:
72189-002
Proprietary Name:
Albuterol Sulfate
Usage Information:
Albuterol (also known as salbutamol) is used to treat wheezing and shortness of breath caused by breathing problems such as asthma. It is a quick-relief medication. Albuterol belongs to a class of drugs known as bronchodilators. It works by relaxing the muscles around the airways so that they open up and you can breathe more easily. Controlling symptoms of breathing problems can decrease time lost from work or school.
11-Digit NDC Billing Format:
72189000225
NDC to RxNorm Crosswalk:
  • RxCUI: 630208 - albuterol sulfate 0.083 % Inhalation Solution
  • RxCUI: 630208 - albuterol 0.83 MG/ML Inhalation Solution
  • RxCUI: 630208 - albuterol 0.083 % Inhalation Solution
  • RxCUI: 630208 - albuterol 0.83 MG/ML (albuterol sulfate 1 MG/ML) Inhalation Solution
  • RxCUI: 630208 - albuterol 2.5 MG per 3 ML Inhalation Solution
    • Labeler Name:
    Direct_rx
    Sample Package:
    No
    Start Marketing Date:
    07-30-2019
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    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 72189-002-25?

    The NDC Packaged Code 72189-002-25 is assigned to a package of 3 ml in 1 bottle of Albuterol Sulfate, labeled by Direct_rx. The product's dosage form is and is administered via form.

    Is NDC 72189-002 included in the NDC Directory?

    No, Albuterol Sulfate with product code 72189-002 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Direct_rx on July 30, 2019 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 72189-002-25?

    The 11-digit format is 72189000225. 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
    5-3-272189-002-255-4-272189-0002-25