Aricept - 62856-247-90 - (donepezil hydrochloride)

Alphabetical Index


Drug Information of Aricept

Product NDC: 62856-247
Proprietary Name: Aricept
Non Proprietary Name: donepezil hydrochloride
Active Ingredient(s): 23    mg/1 & nbsp;   donepezil hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Aricept

Product NDC: 62856-247
Labeler Name: Eisai Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022568
Marketing Category: NDA
Start Marketing Date: 20100723

Package Information of Aricept

Package NDC: 62856-247-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (62856-247-90)

NDC Information of Aricept

NDC Code 62856-247-90
Proprietary Name Aricept
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (62856-247-90)
Product NDC 62856-247
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name donepezil hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100723
Marketing Category Name NDA
Labeler Name Eisai Inc.
Substance Name DONEPEZIL HYDROCHLORIDE
Strength Number 23
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Aricept


General Information