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Donepezil Hydrochloride - 62756-445-65 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 62756-445
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: 62756-445
Labeler Name: Sun Pharmaceutical Industries Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090493
Marketing Category: ANDA
Start Marketing Date: 20110601

Package Information of Donepezil Hydrochloride

Package NDC: 62756-445-65
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (62756-445-65) > 10 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Donepezil Hydrochloride

NDC Code 62756-445-65
Proprietary Name Donepezil Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (62756-445-65) > 10 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 62756-445
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name ANDA
Labeler Name Sun Pharmaceutical Industries 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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