View drug registration information details.

Items	Registration information
ID	420
No	420
Brand Name	ARICEPT EVESS 5 MG
Ingredients	DONEPEZIL HYDROCHLORIDE 5 MG EQ.TO DONEPEZIL FREE BASE 4.56 MG
Dosage Form	TABLET
Primary Packaging	BLISTERPACK
Storage	DO NOT STORE ABOVE 30'C
Shelf Life	3 YEARS
Pack Size	BOX OF 28,30,56,60,98 OR 120 TABLETS
Dispensing Category	Prescription only
ATC Classification	N06DA02
Pharmaceutical Class	DEMENTIA
Indications	SYMPTOMATIC TREATMENT OF MILD, MODERATELY SEVERE AND SEVERE DEMENTIA OF THE ALZHEIMER'S TYPE, VASCULAR DEMENTIA ( DEMENTIA ASSOCIATED WITH CEREBROVASCULAR DISEASE), DEMENTIA WITH LEWY BODIES( DLB).
Contraindications	ARICEPT IS CONTRAINDICATED IN PATIENTS WITH A KNOW HYPERSENSITIVITY TO DONEPEZIL HYDROCHLORIDE, PIPERIDINE DERIVATIVES, OR TO ANY EXCIPIENTS USED IN THE FORMULATION.
Side Effects	THE MOST COMMON ADVERSE EVENTS ARE DIARRHOEA, MUSCLE CRAMPS,FATIGUE, NAUSEA, VOMITING AND INSOMNIA.
Unit Price	-
EDL	No
Description	WHITE, ROUND TABLETS DEBOSSED ARICEPT ON ONE SIDE AND 5 ON THE OTHER
Note
License Owner	DKSH LAOS COMPANY LIMITED
Manufacturer	BUSHU PHARMACEUTICALS LTD. MISATO FACTORY
Country	THAILAND
Import Registration No	1B 5/52( N)
Import Registration Date	2009-11-27
Activity	CERTIFICATE RELEASED
Applied Date	09-ARP-2022
FDD Registration No	03 I 3781/12
FDD Registration Date	2022-09-14
Expiry Date	2025-09-13

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