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  4. NDC Product Code: 0115-2611 Terbutaline Sulfate

NDC 0115-2611 Terbutaline Sulfate

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 0115-2611?
  5. Terbutaline Sulfate Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0115-2611
Proprietary Name:
Terbutaline Sulfate
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amneal Pharmaceuticals Of New York Llc
Labeler Code:
0115
Product Label ID:
382dcebb-6e41-4335-818d-b5822e3fb884
Start Marketing Date: [9]
06-26-2001
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - OFF-WHITE)
Shape:
OVAL (C48345)
Size(s):
11 MM
Imprint(s):
G;2611
Score:
1

Product Packages

NDC Code 0115-2611-01

Package Description: 100 TABLET in 1 BOTTLE

Price per Unit: $1.59996 per EA

NDC Code 0115-2611-02

Package Description: 500 TABLET in 1 BOTTLE

NDC Code 0115-2611-03

Package Description: 1000 TABLET in 1 BOTTLE

Product Details

What is NDC 0115-2611?

The NDC code 0115-2611 is assigned by the FDA to the product Terbutaline Sulfate which is product labeled by Amneal Pharmaceuticals Of New York Llc. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 0115-2611-01 100 tablet in 1 bottle , 0115-2611-02 500 tablet in 1 bottle , 0115-2611-03 1000 tablet in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Terbutaline Sulfate?

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.

Which are Terbutaline Sulfate UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Terbutaline Sulfate Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Terbutaline Sulfate?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Patient Education

Terbutaline


Terbutaline is used to prevent and treat wheezing, shortness of breath, and chest tightness caused by asthma, chronic bronchitis, and emphysema. Terbutaline is in a class of medications called beta agonists. It works by relaxing and opening the airways, making it easier to breathe.
[Learn More]


* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".