NDC 42495-170 Hydroxyzine Pamoate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42495 - Westwood Manufacturing
- 42495-170 - Hydroxyzine Pamoate
Product Characteristics
WHITE (C48325 - BLACK)
Product Packages
NDC Code 42495-170-30
Package Description: 30 CAPSULE in 1 BLISTER PACK
Product Details
What is NDC 42495-170?
What are the uses for Hydroxyzine Pamoate?
Which are Hydroxyzine Pamoate UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROXYZINE PAMOATE (UNII: M20215MUFR)
- HYDROXYZINE (UNII: 30S50YM8OG) (Active Moiety)
Which are Hydroxyzine Pamoate 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)
- STARCH, CORN (UNII: O8232NY3SJ)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Hydroxyzine Pamoate?
- RxCUI: 995278 - hydrOXYzine pamoate 50 MG Oral Capsule
- RxCUI: 995278 - hydroxyzine pamoate 50 MG Oral Capsule
- RxCUI: 995278 - hydroxyzine pamoate 50 MG (hydroxyzine pamoate 85.2 MG eqv to hydroxyzine HCl 50 MG) Oral Capsule
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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".