Home > National Drug Code (NDC) > Donepezil Hydrochloride

Donepezil Hydrochloride - 54868-6207-0 - (Donepezil Hydrochloride)

Alphabetical Index


Drug Information of Donepezil Hydrochloride

Product NDC: 54868-6207
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: 54868-6207
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076786
Marketing Category: ANDA
Start Marketing Date: 20101207

Package Information of Donepezil Hydrochloride

Package NDC: 54868-6207-0
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-6207-0)

NDC Information of Donepezil Hydrochloride

NDC Code 54868-6207-0
Proprietary Name Donepezil Hydrochloride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-6207-0)
Product NDC 54868-6207
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Donepezil Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101207
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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