NDC 67668-161 Cetirizine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67668 - Unique Pharmaceutical Laboratories
- 67668-161 - Cetirizine Hydrochloride
Product Characteristics
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?
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:
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Cetirizine Hydrochloride?
- RxCUI: 1014676 - cetirizine HCl 5 MG Oral Tablet
- RxCUI: 1014676 - cetirizine hydrochloride 5 MG Oral Tablet
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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".