NDC 59651-408 Memantine Hydrochloride
Kit - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59651 - Aurobindo Pharma Limited
- 59651-408 - Memantine Hydrochloride
Product Characteristics
YELLOW (C48330 - YELLOW OPAQUE BODY)
GREEN (C48329 - DARK GREEN OPAQUE BODY)
WHITE (C48325 - WHITE TO OFF-WHITE CAP)
GREEN (C48329 - DARK GREEN OPAQUE CAP)
16 MM
M;14
M;21
M;28
Product Packages
NDC Code 59651-408-28
Package Description: 1 BLISTER PACK in 1 CARTON / 1 KIT in 1 BLISTER PACK
Product Details
What is NDC 59651-408?
What are the uses for Memantine Hydrochloride?
Which are Memantine Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- MEMANTINE HYDROCHLORIDE (UNII: JY0WD0UA60)
- MEMANTINE (UNII: W8O17SJF3T) (Active Moiety)
Which are Memantine 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:
- ETHYLCELLULOSE (20 MPA.S) (UNII: BJG0S321QY)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- HYPROMELLOSE 2910 (15 MPA.S) (UNII: 36SFW2JZ0W)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- STARCH, CORN (UNII: O8232NY3SJ)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- SHELLAC (UNII: 46N107B71O)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Memantine Hydrochloride?
- 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: 996603 - memantine HCl 21 MG 24HR Extended Release Oral Capsule
- RxCUI: 996603 - 24 HR memantine hydrochloride 21 MG Extended Release Oral Capsule
* 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.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[6] What is the FDA Application Number? - This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".