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  4. NDC Product Code: 62756-523 Desloratadine

NDC 62756-523 Desloratadine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 62756-523?
  5. Desloratadine 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:
62756-523
Proprietary Name:
Desloratadine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Sun Pharmaceutical Industries, Inc.
Labeler Code:
62756
Product Label ID:
58ba2dc8-10c2-4532-92e2-40ec2fee3378
Start Marketing Date: [9]
11-24-2010
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
BLUE (C48333)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
5
Score:
1

Product Packages

NDC Code 62756-523-08

Package Description: 100 TABLET, FILM COATED in 1 BOTTLE

NDC Code 62756-523-13

Package Description: 500 TABLET, FILM COATED in 1 BOTTLE

Price per Unit: $0.46246 per EA

NDC Code 62756-523-18

Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE

NDC Code 62756-523-83

Package Description: 30 TABLET, FILM COATED in 1 BOTTLE

NDC Code 62756-523-88

Package Description: 100 TABLET, FILM COATED in 1 BOTTLE

Price per Unit: $0.34352 per EA

Product Details

What is NDC 62756-523?

The NDC code 62756-523 is assigned by the FDA to the product Desloratadine which is product labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is . The product is distributed in 5 packages with assigned NDC codes 62756-523-08 100 tablet, film coated in 1 bottle , 62756-523-13 500 tablet, film coated in 1 bottle , 62756-523-18 1000 tablet, film coated in 1 bottle , 62756-523-83 30 tablet, film coated in 1 bottle , 62756-523-88 100 tablet, film coated 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 Desloratadine?

Desloratadine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, sneezing, hives, and itching. It works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction.

Which are Desloratadine UNII Codes?

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

Which are Desloratadine 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 Desloratadine?

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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Patient Education

Desloratadine


Desloratadine is used in adults and children to relieve hay fever and allergy symptoms, including sneezing; runny nose; and red, itchy, tearing eyes. It is also used to relieve symptoms of urticaria (hives; red, itchy raised areas of the skin), including itching and rash. Desloratadine is in a class of medications called antihistamines. It works by blocking histamine, a substance in the body that causes allergic symptoms.
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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".