NDC 72994-001 Generic Drug
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72994 - Ningbo Shouzheng Medicinal Research Co., Ltd
- 72994-001 - Generic Drug
Product Characteristics
Product Packages
NDC Code 72994-001-11
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 72994-001?
What are the uses for Generic Drug?
Which are Generic Drug UNII Codes?
The UNII codes for the active ingredients in this product are:
- MEMANTINE HYDROCHLORIDE (UNII: JY0WD0UA60)
- MEMANTINE (UNII: W8O17SJF3T) (Active Moiety)
Which are Generic Drug 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:
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- TRIACETIN (UNII: XHX3C3X673)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
What is the NDC to RxNorm Crosswalk for Generic Drug?
- RxCUI: 996561 - memantine HCl 10 MG Oral Tablet
- RxCUI: 996561 - memantine hydrochloride 10 MG Oral Tablet
- RxCUI: 996571 - memantine HCl 5 MG Oral Tablet
- RxCUI: 996571 - memantine hydrochloride 5 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Memantine
Memantine is used to treat the symptoms of Alzheimer's disease (AD; a brain disease that slowly destroys the memory and the ability to think, learn, communicate and handle daily activities). Memantine is in a class of medications called NMDA receptor antagonists. It works by decreasing abnormal activity in the brain. Memantine may improve the ability to think and remember or may slow the loss of these abilities in people who have AD. However, memantine will not cure AD or prevent the loss of these abilities at some time in the future.
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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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".