NDC 71335-0789 Levocetirizine Dihydrochloride

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:
71335-0789
Proprietary Name:
Levocetirizine Dihydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bryant Ranch Prepack
Labeler Code:
71335
Start Marketing Date: [9]
06-29-2012
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
6 MM
Imprint(s):
161;H
Score:
2

Product Packages

NDC Code 71335-0789-1

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 71335-0789-2

Package Description: 90 TABLET in 1 BOTTLE

NDC Code 71335-0789-3

Package Description: 28 TABLET in 1 BOTTLE

NDC Code 71335-0789-4

Package Description: 60 TABLET in 1 BOTTLE

Product Details

What is NDC 71335-0789?

The NDC code 71335-0789 is assigned by the FDA to the product Levocetirizine Dihydrochloride which is product labeled by Bryant Ranch Prepack. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 71335-0789-1 30 tablet in 1 bottle , 71335-0789-2 90 tablet in 1 bottle , 71335-0789-3 28 tablet in 1 bottle , 71335-0789-4 60 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 Levocetirizine Dihydrochloride?

Levocetirizine is an antihistamine used to relieve allergy symptoms such as watery eyes, runny nose, itching eyes/nose, and sneezing. It is also used to relieve itching and hives. It works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction. Levocetirizine does not prevent hives or prevent/treat a serious allergic reaction (such as anaphylaxis). If your doctor has prescribed epinephrine to treat allergic reactions, always carry your epinephrine injector with you. Do not use levocetirizine in place of your epinephrine.

Which are Levocetirizine Dihydrochloride UNII Codes?

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

  • LEVOCETIRIZINE DIHYDROCHLORIDE (UNII: SOD6A38AGA)
  • LEVOCETIRIZINE (UNII: 6U5EA9RT2O) (Active Moiety)

Which are Levocetirizine Dihydrochloride 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 Levocetirizine Dihydrochloride?

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:
  • RxCUI: 855172 - levocetirizine dihydrochloride 5 MG Oral Tablet
  • RxCUI: 855172 - levocetirizine dihydrochloride 5 MG 24 HR Oral Tablet

* Please review the disclaimer below.

Patient Education

Levocetirizine


Levocetirizine is used to relieve runny nose; sneezing; and redness, itching, and tearing of the eyes caused by hay fever, seasonal allergies, and allergies to other substances such as dust mites, animal dander, and mold. It is also used to treat symptoms of hives, including itching and rash. Levocetirizine is in a class of medications called antihistamines. It works by blocking the action of histamine, a substance in the body that causes allergic symptoms.
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* 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".