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Donepezil Hydrochloride - 13668-102-10 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 13668-102
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: 13668-102
Labeler Name: Torrent Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090686
Marketing Category: ANDA
Start Marketing Date: 20110528

Package Information of Donepezil Hydrochloride

Package NDC: 13668-102-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (13668-102-10)

NDC Information of Donepezil Hydrochloride

NDC Code 13668-102-10
Proprietary Name Donepezil Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (13668-102-10)
Product NDC 13668-102
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110528
Marketing Category Name ANDA
Labeler Name Torrent Pharmaceuticals Limited
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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