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donepezil hydrochloride - 59762-0245-2 - (DONEPEZIL HYDROCHLORIDE)

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Drug Information of donepezil hydrochloride

Product NDC: 59762-0245
Proprietary Name: donepezil hydrochloride
Non Proprietary Name: DONEPEZIL HYDROCHLORIDE
Active Ingredient(s): 5    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: 59762-0245
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020690
Marketing Category: NDA
Start Marketing Date: 19961126

Package Information of donepezil hydrochloride

Package NDC: 59762-0245-2
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (59762-0245-2)

NDC Information of donepezil hydrochloride

NDC Code 59762-0245-2
Proprietary Name donepezil hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (59762-0245-2)
Product NDC 59762-0245
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DONEPEZIL HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19961126
Marketing Category Name NDA
Labeler Name Greenstone LLC
Substance Name DONEPEZIL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of donepezil hydrochloride


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