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Donepezil Hydrochloride - 67046-129-30 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 67046-129
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: 67046-129
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020690
Marketing Category: NDA
Start Marketing Date: 20110131

Package Information of Donepezil Hydrochloride

Package NDC: 67046-129-30
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-129-30)

NDC Information of Donepezil Hydrochloride

NDC Code 67046-129-30
Proprietary Name Donepezil Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-129-30)
Product NDC 67046-129
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110131
Marketing Category Name NDA
Labeler Name Contract Pharmacy Services-PA
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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