NDC 44237-001 Linkus Lozenges Cough Suppressant/oral Anesthetic

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
44237-001
Proprietary Name:
Linkus Lozenges Cough Suppressant/oral Anesthetic
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Herbion Pakistan (pvt.) Ltd.
Labeler Code:
44237
Start Marketing Date: [9]
04-01-2010
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
YELLOW (C48330)
Shape:
ROUND (C48348)
Size(s):
17 MM
Imprint(s):
NONE
Score:
1
Flavor(s):
PINEAPPLE (C73409)

Product Packages

NDC Code 44237-001-08

Package Description: 8 LOZENGE in 1 BOX

Product Details

What is NDC 44237-001?

The NDC code 44237-001 is assigned by the FDA to the product Linkus Lozenges Cough Suppressant/oral Anesthetic which is product labeled by Herbion Pakistan (pvt.) Ltd.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 44237-001-08 8 lozenge in 1 box . 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 Linkus Lozenges Cough Suppressant/oral Anesthetic?

Uses:Temporarily relieves cough due to minor throat and bronchial irritation associated with the common coldFor temporary relief of occasional minor irritation, pain, sore mouth and sore throat

Which are Linkus Lozenges Cough Suppressant/oral Anesthetic UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Linkus Lozenges Cough Suppressant/oral Anesthetic?

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 code indicates a single concept unique identifier (RXCUI) is associated with this product:

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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".