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Donepezil Hydrochloride - 16714-385-02 - (Donepezil Hydrochloride)

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Drug Information of Donepezil Hydrochloride

Product NDC: 16714-385
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: 16714-385
Labeler Name: NorthStar RxLLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201724
Marketing Category: ANDA
Start Marketing Date: 20130219

Package Information of Donepezil Hydrochloride

Package NDC: 16714-385-02
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (16714-385-02)

NDC Information of Donepezil Hydrochloride

NDC Code 16714-385-02
Proprietary Name Donepezil Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (16714-385-02)
Product NDC 16714-385
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130219
Marketing Category Name ANDA
Labeler Name NorthStar RxLLC
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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