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  5. NDC Package Code: 70518-1230-0 Proair Hfa

NDC Package 70518-1230-0 Proair Hfa

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:
70518-1230-0
Package Description:
1 INHALER in 1 CARTON / 200 AEROSOL, METERED in 1 INHALER
Product Code:
70518-1230
Proprietary Name:
Proair Hfa
Usage Information:
Albuterol (also known as salbutamol) is used to prevent and treat wheezing and shortness of breath caused by breathing problems (such as asthma, chronic obstructive pulmonary disease). It is also used to prevent asthma brought on by exercise. It is a quick-relief drug. 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:
70518123000
NDC to RxNorm Crosswalk:
  • RxCUI: 2123072 - albuterol 90 MCG/INHAL Metered Dose Inhaler, 200 Actuations, generic for ProAir
  • RxCUI: 2123072 - NDA021457 200 ACTUAT albuterol 0.09 MG/ACTUAT Metered Dose Inhaler
  • RxCUI: 2123072 - albuterol 90 MCG/ACTUAT Metered Dose Inhaler, 200 Actuations, generic for ProAir
  • RxCUI: 745752 - ProAir HFA 90 MCG/INHAL Metered Dose Inhaler, 200 Actuations
  • RxCUI: 745752 - NDA021457 200 ACTUAT albuterol 0.09 MG/ACTUAT Metered Dose Inhaler [ProAir]
    • Labeler Name:
    Remedyrepack Inc.
    Sample Package:
    No
    Start Marketing Date:
    05-29-2018
    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 70518-1230-0?

    The NDC Packaged Code 70518-1230-0 is assigned to a package of 1 inhaler in 1 carton / 200 aerosol, metered in 1 inhaler of Proair Hfa, labeled by Remedyrepack Inc.. The product's dosage form is and is administered via form.

    Is NDC 70518-1230 included in the NDC Directory?

    No, Proair Hfa with product code 70518-1230 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Remedyrepack Inc. on May 29, 2018 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 70518-1230-0?

    The 11-digit format is 70518123000. 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 5-4-1 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
    5-4-170518-1230-05-4-270518-1230-00