Home > National Drug Code (NDC) > donepezil hydrochloride

donepezil hydrochloride - 59762-0250-1 - (DONEPEZIL HYDROCHLORIDE)

Alphabetical Index


Drug Information of donepezil hydrochloride

Product NDC: 59762-0250
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, ORALLY DISINTEGRATING
Coding System: National Drug Codes(NDC)

Labeler Information of donepezil hydrochloride

Product NDC: 59762-0250
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021720
Marketing Category: NDA
Start Marketing Date: 20041018

Package Information of donepezil hydrochloride

Package NDC: 59762-0250-1
Package Description: 3 BLISTER PACK in 1 CARTON (59762-0250-1) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Information of donepezil hydrochloride

NDC Code 59762-0250-1
Proprietary Name donepezil hydrochloride
Package Description 3 BLISTER PACK in 1 CARTON (59762-0250-1) > 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Product NDC 59762-0250
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name DONEPEZIL HYDROCHLORIDE
Dosage Form Name TABLET, ORALLY DISINTEGRATING
Route Name ORAL
Start Marketing Date 20041018
Marketing Category Name NDA
Labeler Name Greenstone LLC
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