View drug registration information details.
Items | Registration information |
ID | 501 |
No | 501 |
Brand Name | ARICEPT EVESS 10 MG |
Ingredients | DONEPEZIL HYDROCHLORIDE 10 MG EQ.TO DONEPEZIL FREE BASE 9.12 MG |
Dosage Form | TABLET |
Primary Packaging | BLISTERPACK |
Storage | |
Shelf Life | 3 YEARS |
Pack Size | BOX OF 28,30,56,60,98 OR 120 TABLETS. |
Dispensing Category | |
ATC Classification | |
Pharmaceutical Class | |
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 | |
Side Effects | |
Unit Price | |
EDL |
NULL |
Description | YELLOW, ROUND TABLETS DEBOSSED ARICEPT ON ONE SIDE AND 10 ON THE OTHER SIDE |
Note | |
License Owner | DKSH LAOS COMPANY LIMITED |
Manufacturer | BUSHU PHARMACEUTICALS LTD. MISATO FACTORY |
Country | THAILAND |
Import Registration No | |
Import Registration Date | |
Activity | STEP 1: RECEIVE (RENEW) |
Applied Date | 28-APR-2025 |
FDD Registration No | 03 I 3780/12 |
FDD Registration Date | 14-SEP-2022 |
Expiry Date | 13-SEP-2025 |
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