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  5. NDC Package Code: 72843-101-10 Terbutaline Sulfate

NDC Package 72843-101-10 Terbutaline Sulfate

Injection Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
72843-101-10
Package Description:
10 VIAL in 1 BOX / 1 mL in 1 VIAL
Product Code:
72843-101
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:
72843010110
NDC to RxNorm Crosswalk:
  • RxCUI: 857635 - terbutaline sulfate 1 MG in 1 ML Injection
  • RxCUI: 857635 - 1 ML terbutaline sulfate 1 MG/ML Injection
  • RxCUI: 857635 - terbutaline sulfate 1 MG per 1 ML Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Ubi Pharma Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • TERBUTALINE SULFATE 1 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    ANDA200122
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    12-15-2014
    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 72843-101-10?

    The NDC Packaged Code 72843-101-10 is assigned to a package of 10 vial in 1 box / 1 ml in 1 vial of Terbutaline Sulfate, a human prescription drug labeled by Ubi Pharma Inc.. The product's dosage form is injection and is administered via subcutaneous form.

    Is NDC 72843-101 included in the NDC Directory?

    Yes, Terbutaline Sulfate with product code 72843-101 is active and included in the NDC Directory. The product was first marketed by Ubi Pharma Inc. on December 15, 2014 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 72843-101-10?

    The 11-digit format is 72843010110. 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
    5-3-272843-101-105-4-272843-0101-10