NDC 67296-1660 Hydroxyzine Pamoate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67296 - Redpharm Drug, Inc.
- 67296-1660 - Hydroxyzine Pamoate
Product Characteristics
Product Packages
NDC Code 67296-1660-3
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 67296-1660-7
Package Description: 15 CAPSULE in 1 BOTTLE
Product Details
What is NDC 67296-1660?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GELATIN (UNII: 2G86QN327L)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- STARCH, CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Hydroxyzine Pamoate?
- RxCUI: 995253 - hydrOXYzine pamoate 25 MG Oral Capsule
- RxCUI: 995253 - hydroxyzine pamoate 25 MG Oral Capsule
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Patient Education
Hydroxyzine
Hydroxyzine is used in adults and children to relieve itching caused by allergic skin reactions. It is also used alone or with other medications in adults and children to relieve anxiety and tension. Hydroxyzine is also used along with other medications in adults and children as a sedative before and after general anesthesia for surgery. Hydroxyzine 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. It also works by decreasing activity in the brain.
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* Please review the disclaimer below.
[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".