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  4. NDC Product Code: 53113-215 Broncomar

NDC 53113-215 Broncomar

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 53113-215?
  4. Broncomar Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
53113-215
Proprietary Name:
Broncomar
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Gadal Laboratories Inc
Labeler Code:
53113
Product Label ID:
058cdaf3-ed98-44b2-9ecc-fd810dcac12e
Start Marketing Date: [9]
06-01-2014
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 53113-215-06

Package Description: 1 BOTTLE in 1 CARTON / 177 mL in 1 BOTTLE

Product Details

What is NDC 53113-215?

The NDC code 53113-215 is assigned by the FDA to the product Broncomar which is product labeled by Gadal Laboratories Inc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 53113-215-06 1 bottle in 1 carton / 177 ml 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 Broncomar?

UsesFor temporary relief of bronchial and nasal congestionHelp loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make cough more productive.Teporarily relieves cough due to minor throat and bronchial irritation as may occur with the common cold

Which are Broncomar UNII Codes?

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

Which are Broncomar 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:

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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".