Aricept - 63629-3632-2 - (donepezil hydrochloride)

Alphabetical Index


Drug Information of Aricept

Product NDC: 63629-3632
Proprietary Name: Aricept
Non Proprietary Name: donepezil hydrochloride
Active Ingredient(s): 10    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: 63629-3632
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020690
Marketing Category: NDA
Start Marketing Date: 19961125

Package Information of Aricept

Package NDC: 63629-3632-2
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (63629-3632-2)

NDC Information of Aricept

NDC Code 63629-3632-2
Proprietary Name Aricept
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (63629-3632-2)
Product NDC 63629-3632
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name donepezil hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19961125
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name DONEPEZIL HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Aricept


General Information