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donepezil hydrochloride - 55154-0536-0 - (DONEPEZIL HYDROCHLORIDE)

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Drug Information of donepezil hydrochloride

Product NDC: 55154-0536
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: 55154-0536
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020690
Marketing Category: NDA
Start Marketing Date: 19961126

Package Information of donepezil hydrochloride

Package NDC: 55154-0536-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0536-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of donepezil hydrochloride

NDC Code 55154-0536-0
Proprietary Name donepezil hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-0536-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-0536
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DONEPEZIL HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19961126
Marketing Category Name NDA
Labeler Name Cardinal Health
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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