View the LUCIPOMA registration information details.
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ItemsDrug Registration information
ID1771
No1771
Brand NameLUCIPOMA
IngredientsPOMALIDOMIDE 4 MG
Dosage FormCAPSULE
Primary PackagingBOTTLE
Storage
Shelf Life2 YEARS
Pack SizeBOX OF 21'S/BOTTLE
Dispensing Category
ATC Classification
Pharmaceutical Class
IndicationsFOR THE TREATMENT OF ADULT PATIENTS: IN COMBINATION WITH DEXAMETHASONE, FOR PATIENTS WITH MULTIPLE MYELOMA WHO HAVE RECEIVED AT LEAST 2 PRIOR THERAPIES INCLUDING LENALIDOMIDE AND PROTEASOME INHIBITOR AND HAVE DEMONSTRATED DISEASE PROGRESSION ON OR WITHIN 60 DAYS OF COMPLETEION OF LAST THERAPY
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionWHITE CAPSULE CONTAINS YELLOW POWDER
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 No12 L 1283/24
FDD Registration Date23/01/2025
Expiry Date22/01/2030
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