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Donepezil Hydrochloride - 0093-0739-56 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 0093-0739
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: 0093-0739
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090425
Marketing Category: ANDA
Start Marketing Date: 20110531

Package Information of Donepezil Hydrochloride

Package NDC: 0093-0739-56
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0093-0739-56)

NDC Information of Donepezil Hydrochloride

NDC Code 0093-0739-56
Proprietary Name Donepezil Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0093-0739-56)
Product NDC 0093-0739
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 Teva Pharmaceuticals USA Inc
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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