NDC 67668-161 Cetirizine Hydrochloride

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:
67668-161
Proprietary Name:
Cetirizine Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Unique Pharmaceutical Laboratories
Labeler Code:
67668
Start Marketing Date: [9]
10-01-2009
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE)
Shape:
BULLET (C48335)
Size(s):
7 MM
Imprint(s):
CTN;5
Score:
1

Product Packages

NDC Code 67668-161-00

Package Description: 100 TABLET in 1 BOTTLE

NDC Code 67668-161-30

Package Description: 30 TABLET in 1 BOTTLE

NDC Code 67668-161-45

Package Description: 45 TABLET in 1 BOTTLE

Product Details

What is NDC 67668-161?

The NDC code 67668-161 is assigned by the FDA to the product Cetirizine Hydrochloride which is product labeled by Unique Pharmaceutical Laboratories. The product's dosage form is . The product is distributed in 3 packages with assigned NDC codes 67668-161-00 100 tablet in 1 bottle , 67668-161-30 30 tablet in 1 bottle , 67668-161-45 45 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 Cetirizine Hydrochloride?

Adults and children 6 years and over1 to 2 tablets once daily depending upon severity of symptoms; do not take more than 2 tablets in 24 hours.Adults 65 years and over1 tablet1 tablet once a day; do not take more than 1 tablet in 24 hours.Children under 6 years of ageAsk a doctorConsumers with liver or kidney diseaseAsk a doctor

Which are Cetirizine Hydrochloride UNII Codes?

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

Which are Cetirizine Hydrochloride 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 Cetirizine Hydrochloride?

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:

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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".