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Donepezil Hydrochloride - 65862-326-99 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 65862-326
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: 65862-326
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090056
Marketing Category: ANDA
Start Marketing Date: 20110531

Package Information of Donepezil Hydrochloride

Package NDC: 65862-326-99
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (65862-326-99)

NDC Information of Donepezil Hydrochloride

NDC Code 65862-326-99
Proprietary Name Donepezil Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (65862-326-99)
Product NDC 65862-326
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110531
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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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