Home > National Drug Code (NDC) > DONEPEZIL HYDROCHLORIDE

DONEPEZIL HYDROCHLORIDE - 59746-329-90 - (DONEPEZIL HYDROCHLORIDE)

Alphabetical Index


Drug Information of DONEPEZIL HYDROCHLORIDE

Product NDC: 59746-329
Proprietary Name: DONEPEZIL HYDROCHLORIDE
Non Proprietary Name: DONEPEZIL HYDROCHLORIDE
Active Ingredient(s): 5    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: 59746-329
Labeler Name: Jubilant Cadista Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090768
Marketing Category: ANDA
Start Marketing Date: 20110529

Package Information of DONEPEZIL HYDROCHLORIDE

Package NDC: 59746-329-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (59746-329-90)

NDC Information of DONEPEZIL HYDROCHLORIDE

NDC Code 59746-329-90
Proprietary Name DONEPEZIL HYDROCHLORIDE
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (59746-329-90)
Product NDC 59746-329
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DONEPEZIL HYDROCHLORIDE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110529
Marketing Category Name ANDA
Labeler Name Jubilant Cadista Pharmaceuticals Inc.
Substance Name DONEPEZIL HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]

Complete Information of DONEPEZIL HYDROCHLORIDE


General Information