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Donepezil Hydrochloride - 0781-5275-13 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 0781-5275
Proprietary Name: Donepezil Hydrochloride
Non Proprietary Name: Donepezil Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Donepezil Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Donepezil Hydrochloride

Product NDC: 0781-5275
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090290
Marketing Category: ANDA
Start Marketing Date: 20110531

Package Information of Donepezil Hydrochloride

Package NDC: 0781-5275-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-5275-13) > 10 TABLET in 1 BLISTER PACK

NDC Information of Donepezil Hydrochloride

NDC Code 0781-5275-13
Proprietary Name Donepezil Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (0781-5275-13) > 10 TABLET in 1 BLISTER PACK
Product NDC 0781-5275
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110531
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name DONEPEZIL HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of Donepezil Hydrochloride


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