1. Home
  2. Labeler Index
  3. Rebel Distributors Corp
  4. 21695-198
  5. NDC Package Code: 21695-198-01 Albuterol

NDC Package 21695-198-01 Albuterol

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:
21695-198-01
Package Description:
200 AEROSOL, METERED in 1 CANISTER
Product Code:
21695-198
Proprietary Name:
Albuterol
Usage Information:
Albuterol Inhalation Aerosol is indicated for the prevention and relief of bronchospasm in patients 4 years of age and older with reversible obstructive airway disease, and for the prevention of exercise induced bronchospasm in patients 4 years of age and older.Albuterol Inhalation Aerosol can be used with or without concomitant steroid therapy.
11-Digit NDC Billing Format:
21695019801
NDC to RxNorm Crosswalk:
  • RxCUI: 745679 - albuterol sulfate 90 MCG/INHAL Metered Dose Inhaler, 200 Actuations
  • RxCUI: 745679 - 200 ACTUAT albuterol 0.09 MG/ACTUAT Metered Dose Inhaler
  • RxCUI: 745679 - albuterol 0.09 MG/ACTUAT 200 ACTUAT Metered Dose Inhaler
  • RxCUI: 745679 - albuterol 90 MCG/ACTUAT (albuterol sulfate 108 MCG/ACTUAT from mouthpiece) 200 ACTUAT Metered Dose Inhaler
  • RxCUI: 745679 - albuterol 90 MCG/ACTUAT Metered Dose Inhaler, 200 ACTUAT
    • Labeler Name:
    Rebel Distributors Corp
    Sample Package:
    No
    Start Marketing Date:
    08-14-1996
    Listing Expiration Date:
    12-31-2017
    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 21695-198-01?

    The NDC Packaged Code 21695-198-01 is assigned to a package of 200 aerosol, metered in 1 canister of Albuterol, labeled by Rebel Distributors Corp. The product's dosage form is and is administered via form.

    Is NDC 21695-198 included in the NDC Directory?

    No, Albuterol with product code 21695-198 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Rebel Distributors Corp on August 14, 1996 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 21695-198-01?

    The 11-digit format is 21695019801. 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
    5-3-221695-198-015-4-221695-0198-01