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Donepezil Hydrochloride - 33342-030-07 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 33342-030
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, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of Donepezil Hydrochloride

Product NDC: 33342-030
Labeler Name: Macleods Pharmaceuticals Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201146
Marketing Category: ANDA
Start Marketing Date: 20121214

Package Information of Donepezil Hydrochloride

Package NDC: 33342-030-07
Package Description: 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (33342-030-07)

NDC Information of Donepezil Hydrochloride

NDC Code 33342-030-07
Proprietary Name Donepezil Hydrochloride
Package Description 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (33342-030-07)
Product NDC 33342-030
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20121214
Marketing Category Name ANDA
Labeler Name Macleods Pharmaceuticals 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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