View the LUCIRUX registration information details.
Back to drug list
ItemsDrug Registration information
ID1786
No1786
Brand NameLUCIRUX
IngredientsRUXOLITINIB 5 MG
Dosage FormTABLET
Primary PackagingBOTTLE
Storage
Shelf Life2 YEARS
Pack SizeBOX OF 60'S/BOTTLE
Dispensing Category
ATC Classification
Pharmaceutical Class
IndicationsFOR THE TREATMENT OF INTERMEDIATE OR HIGH RISK MYELOFIBROSIS, INCLUDING PRIMARY MYELOFIBROSIS, POST-POLYCYTHEMIA VERA MYELOFIBROSIS AND POST-ESSENTIAL THROMBOCYTHEMIA MYELOFIBROSIS
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionWHITE TABLET, WITH LETTER LUS ON ONE SIDE AND PLAIN ON THE OTHER SIDE
Note
License OwnerLUCIUS PHARMACEUTICALS(LAO) CO.,LTD
ManufacturerLUCIUS PHARMACEUTICALS(LAO) CO.,LTD
CountryLAOS
Import Registration No
Import Registration Date
ActivityCERTIFICATE RELEASED
Applied Date
FDD Registration No03 L 1323/25
FDD Registration Date07/04/2025
Expiry Date06/04/2030
Back to drug list
ADB ASEAN COVID-19 Laos JICA KOICA Global Fund WFP UHS Laos World Bank MOH Laos UNODC WHO SIDA