Home > National Drug Code (NDC) > DONEPEZIL HYDROCHLORIDE

DONEPEZIL HYDROCHLORIDE - 16729-124-10 - (DONEPEZIL HYDROCHLORIDE)

Alphabetical Index


Drug Information of DONEPEZIL HYDROCHLORIDE

Product NDC: 16729-124
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: 16729-124
Labeler Name: Accord Healthcare, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201335
Marketing Category: ANDA
Start Marketing Date: 20111231

Package Information of DONEPEZIL HYDROCHLORIDE

Package NDC: 16729-124-10
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (16729-124-10)

NDC Information of DONEPEZIL HYDROCHLORIDE

NDC Code 16729-124-10
Proprietary Name DONEPEZIL HYDROCHLORIDE
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (16729-124-10)
Product NDC 16729-124
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DONEPEZIL HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20111231
Marketing Category Name ANDA
Labeler Name Accord Healthcare, 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


General Information