NDC 52959-923 Cetirizine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 52959 - H. J. Harkins Company Inc.
- 52959-923 - Cetirizine Hydrochloride
Product Characteristics
Product Packages
NDC Code 52959-923-07
Package Description: 7 TABLET in 1 CONTAINER
NDC Code 52959-923-10
Package Description: 10 TABLET in 1 CONTAINER
NDC Code 52959-923-14
Package Description: 14 TABLET in 1 CONTAINER
NDC Code 52959-923-15
Package Description: 15 TABLET in 1 CONTAINER
NDC Code 52959-923-20
Package Description: 20 TABLET in 1 CONTAINER
NDC Code 52959-923-30
Package Description: 30 TABLET in 1 CONTAINER
NDC Code 52959-923-60
Package Description: 60 TABLET in 1 CONTAINER
NDC Code 52959-923-90
Package Description: 90 TABLET in 1 CONTAINER
Product Details
What is NDC 52959-923?
What are the uses for Cetirizine Hydrochloride?
Which are Cetirizine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA)
- CETIRIZINE (UNII: YO7261ME24) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Cetirizine Hydrochloride?
- RxCUI: 1014678 - cetirizine HCl 10 MG Oral Tablet
- RxCUI: 1014678 - cetirizine hydrochloride 10 MG Oral Tablet
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Patient Education
Cetirizine Injection
Cetirizine injection is used to treat acute urticaria in adults and children 6 months of age or older. Cetirizine 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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[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".