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Donepezil Hydrochloride - 0781-5276-64 - (donepezil hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 0781-5276
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, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Donepezil Hydrochloride

Product NDC: 0781-5276
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091198
Marketing Category: ANDA
Start Marketing Date: 20110510

Package Information of Donepezil Hydrochloride

Package NDC: 0781-5276-64
Package Description: 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0781-5276-64)

NDC Information of Donepezil Hydrochloride

NDC Code 0781-5276-64
Proprietary Name Donepezil Hydrochloride
Package Description 30 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (0781-5276-64)
Product NDC 0781-5276
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name donepezil hydrochloride
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20110510
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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