NDC 68258-8907 Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68258 - Dispensing Solutions, Inc.
- 68258-8907 - Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride
Product Characteristics
Product Packages
NDC Code 68258-8907-2
Package Description: 4 BLISTER PACK in 1 CARTON / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
Product Details
What is NDC 68258-8907?
What are the uses for Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride?
Which are Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA)
- CETIRIZINE (UNII: YO7261ME24) (Active Moiety)
- PSEUDOEPHEDRINE HYDROCHLORIDE (UNII: 6V9V2RYJ8N)
- PSEUDOEPHEDRINE (UNII: 7CUC9DDI9F) (Active Moiety)
Which are Cetirizine Hydrochloride And Pseudoephedrine 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- TALC (UNII: 7SEV7J4R1U)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Cetirizine Hydrochloride And Pseudoephedrine Hydrochloride?
- RxCUI: 1014571 - cetirizine HCl 5 MG / pseudoephedrine HCl 120 MG 12HR Extended Release Oral Tablet
- RxCUI: 1014571 - 12 HR cetirizine hydrochloride 5 MG / pseudoephedrine hydrochloride 120 MG Extended Release Oral Tablet
- RxCUI: 1014571 - cetirizine dihydrochloride 5 MG / pseudoephedrine HCl 120 MG 12 HR Extended Release 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".