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Donepezil Hydrochloride - 52125-492-19 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 52125-492
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Donepezil Hydrochloride

Product NDC: 52125-492
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090493
Marketing Category: ANDA
Start Marketing Date: 20130522

Package Information of Donepezil Hydrochloride

Package NDC: 52125-492-19
Package Description: 90 TABLET, FILM COATED in 1 VIAL (52125-492-19)

NDC Information of Donepezil Hydrochloride

NDC Code 52125-492-19
Proprietary Name Donepezil Hydrochloride
Package Description 90 TABLET, FILM COATED in 1 VIAL (52125-492-19)
Product NDC 52125-492
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130522
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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