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  5. NDC Package Code: 24979-133-03 Terbutaline Sulfate

NDC Package 24979-133-03 Terbutaline Sulfate

Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
24979-133-03
Package Description:
1000 TABLET in 1 BOTTLE
Product Code:
24979-133
Proprietary Name:
Terbutaline Sulfate
Non-Proprietary Name:
Terbutaline Sulfate
Substance Name:
Terbutaline Sulfate
Usage Information:
Terbutaline is used to treat wheezing and shortness of breath from lung problems (e.g., asthma, chronic obstructive pulmonary disease-COPD, bronchitis, emphysema). Terbutaline 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.
11-Digit NDC Billing Format:
24979013303
NDC to RxNorm Crosswalk:
  • RxCUI: 857677 - terbutaline sulfate 2.5 MG Oral Tablet
  • RxCUI: 857683 - terbutaline sulfate 5 MG Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Twi Pharmaceuticals, Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • TERBUTALINE SULFATE 5 mg/1
    • Sample Package:
    No
    FDA Application Number:
    ANDA211832
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    07-13-2020
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    24979-133-01100 TABLET in 1 BOTTLE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 24979-133-03?

    The NDC Packaged Code 24979-133-03 is assigned to a package of 1000 tablet in 1 bottle of Terbutaline Sulfate, a human prescription drug labeled by Twi Pharmaceuticals, Inc.. The product's dosage form is tablet and is administered via oral form.

    Is NDC 24979-133 included in the NDC Directory?

    Yes, Terbutaline Sulfate with product code 24979-133 is active and included in the NDC Directory. The product was first marketed by Twi Pharmaceuticals, Inc. on July 13, 2020 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 11-digit format for NDC 24979-133-03?

    The 11-digit format is 24979013303. 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
    5-3-224979-133-035-4-224979-0133-03