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Donepezil Hydrochloride - 63739-667-10 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 63739-667
Proprietary Name: Donepezil Hydrochloride
Non Proprietary Name: Donepezil Hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Donepezil Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Donepezil Hydrochloride

Product NDC: 63739-667
Labeler Name: McKesson Packaging Services a business unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076786
Marketing Category: ANDA
Start Marketing Date: 20130308

Package Information of Donepezil Hydrochloride

Package NDC: 63739-667-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-667-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Donepezil Hydrochloride

NDC Code 63739-667-10
Proprietary Name Donepezil Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-667-10) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 63739-667
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130308
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services a business unit of McKesson Corporation
Substance Name DONEPEZIL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Donepezil Hydrochloride


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