Home > National Drug Code (NDC) > Donepezil Hydrochloride

Donepezil Hydrochloride - 55648-312-06 - (Donepezil Hydrochloride)

Alphabetical Index


Drug Information of Donepezil Hydrochloride

Product NDC: 55648-312
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: 55648-312
Labeler Name: Wockhardt Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091267
Marketing Category: ANDA
Start Marketing Date: 20110528

Package Information of Donepezil Hydrochloride

Package NDC: 55648-312-06
Package Description: 100 BLISTER PACK in 1 CARTON (55648-312-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of Donepezil Hydrochloride

NDC Code 55648-312-06
Proprietary Name Donepezil Hydrochloride
Package Description 100 BLISTER PACK in 1 CARTON (55648-312-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55648-312
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110528
Marketing Category Name ANDA
Labeler Name Wockhardt 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


General Information