NDC 68151-5829 Namenda Xr
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-5829 - Namenda Xr
Product Characteristics
GREEN (C48329 - DARK GREEN (OPAQUE))
3 MM
FLI;28;MG
Product Packages
NDC Code 68151-5829-8
Package Description: 1 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 68151-5829?
What are the uses for Namenda Xr?
Which are Namenda Xr UNII Codes?
The UNII codes for the active ingredients in this product are:
- MEMANTINE HYDROCHLORIDE (UNII: JY0WD0UA60)
- MEMANTINE (UNII: W8O17SJF3T) (Active Moiety)
Which are Namenda Xr 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:
- SUCROSE (UNII: C151H8M554)
- POVIDONE K30 (UNII: U725QWY32X)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- TALC (UNII: 7SEV7J4R1U)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- ETHYLCELLULOSE (100 MPA.S) (UNII: 47MLB0F1MV)
- AMMONIA (UNII: 5138Q19F1X)
What is the NDC to RxNorm Crosswalk for Namenda Xr?
- RxCUI: 996594 - memantine HCl 14 MG 24HR Extended Release Oral Capsule
- RxCUI: 996594 - 24 HR memantine hydrochloride 14 MG Extended Release Oral Capsule
- RxCUI: 996594 - memantine hydrochloride 14 MG 24 HR Extended Release Oral Capsule
- RxCUI: 996597 - Namenda XR 14 MG 24HR Extended Release Oral Capsule
- RxCUI: 996597 - 24 HR memantine hydrochloride 14 MG Extended Release Oral Capsule [Namenda]
* 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".