NDC 12634-987 Cetirizine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 12634 - Apotheca Inc.
- 12634-987 - Cetirizine Hydrochloride
Product Characteristics
Product Packages
NDC Code 12634-987-00
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC
NDC Code 12634-987-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC
NDC Code 12634-987-50
Package Description: 50 TABLET in 1 BOTTLE, PLASTIC
NDC Code 12634-987-71
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 12634-987-80
Package Description: 20 TABLET in 1 BOTTLE, PLASTIC
NDC Code 12634-987-96
Package Description: 6 TABLET in 1 BOTTLE, PLASTIC
NDC Code 12634-987-97
Package Description: 7 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 12634-987?
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)
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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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".