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donepezil hydrochloride - 68382-303-16 - (donepezil hydrochloride)

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Drug Information of donepezil hydrochloride

Product NDC: 68382-303
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: 68382-303
Labeler Name: Zydus Pharmaceuticals (USA) Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090100
Marketing Category: ANDA
Start Marketing Date: 20110525

Package Information of donepezil hydrochloride

Package NDC: 68382-303-16
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (68382-303-16)

NDC Information of donepezil hydrochloride

NDC Code 68382-303-16
Proprietary Name donepezil hydrochloride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (68382-303-16)
Product NDC 68382-303
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name donepezil hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110525
Marketing Category Name ANDA
Labeler Name Zydus 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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