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Donepezil Hydrochloride - 64679-312-03 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 64679-312
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: 64679-312
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091267
Marketing Category: ANDA
Start Marketing Date: 20110528

Package Information of Donepezil Hydrochloride

Package NDC: 64679-312-03
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (64679-312-03)

NDC Information of Donepezil Hydrochloride

NDC Code 64679-312-03
Proprietary Name Donepezil Hydrochloride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (64679-312-03)
Product NDC 64679-312
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 Wockhardt USA LLC.
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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