NDC 59746-329 Donepezil Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
59746-329
Proprietary Name:
Donepezil Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Jubilant Cadista Pharmaceuticals Inc.
Labeler Code:
59746
Start Marketing Date: [9]
05-31-2011
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE TO OFF-WHITE)
Shape:
ROUND (C48348)
Size(s):
7 MM
Imprint(s):
J;5
Score:
1

Product Packages

NDC Code 59746-329-01

Package Description: 100 TABLET, FILM COATED in 1 BOTTLE

NDC Code 59746-329-03

Package Description: 10 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED in 1 BLISTER PACK (59746-329-12)

NDC Code 59746-329-05

Package Description: 500 TABLET, FILM COATED in 1 BOTTLE

NDC Code 59746-329-10

Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE

NDC Code 59746-329-30

Package Description: 30 TABLET, FILM COATED in 1 BOTTLE

Price per Unit: $0.04682 per EA

NDC Code 59746-329-90

Package Description: 90 TABLET, FILM COATED in 1 BOTTLE

Price per Unit: $0.04682 per EA

Product Details

What is NDC 59746-329?

The NDC code 59746-329 is assigned by the FDA to the product Donepezil Hydrochloride which is product labeled by Jubilant Cadista Pharmaceuticals Inc.. The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 59746-329-01 100 tablet, film coated in 1 bottle , 59746-329-03 10 blister pack in 1 carton / 10 tablet, film coated in 1 blister pack (59746-329-12), 59746-329-05 500 tablet, film coated in 1 bottle , 59746-329-10 1000 tablet, film coated in 1 bottle , 59746-329-30 30 tablet, film coated in 1 bottle , 59746-329-90 90 tablet, film coated in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Donepezil Hydrochloride?

Donepezil hydrochloride tablets, USP are indicated for the treatment of dementia of the Alzheimer's type. Efficacy has been demonstrated in patients with mild, moderate, and severe Alzheimer's disease.

Which are Donepezil Hydrochloride UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Donepezil 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:

What is the NDC to RxNorm Crosswalk for Donepezil Hydrochloride?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

* Please review the disclaimer below.

Patient Education

Donepezil


Donepezil is used to treat dementia (a brain disorder that affects the ability to remember, think clearly, communicate, and perform daily activities and may cause changes in mood and personality) in people who have Alzheimer's disease (AD; a brain disease that slowly destroys the memory and the ability to think, learn, communicate and handle daily activities). Donepezil is in a class of medications called cholinesterase inhibitors. It improves mental function (such as memory, attention, the ability to interact with others, speak, think clearly, and perform regular daily activities) by increasing the amount of a certain naturally occurring substance in the brain. Donepezil may improve the ability to think and remember or slow the loss of these abilities in people who have AD. However, donepezil will not cure AD or prevent the loss of mental abilities at some time in the future.
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* Please review the disclaimer below.

Product Footnotes

[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".