View the ALIGIRITINIB registration information details.
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ItemsDrug Registration information
ID1601
No1601
Brand NameALIGIRITINIB
IngredientsGILTERITINIB FUMARATE 40 MG
Dosage FormTABLET
Primary PackagingBOTTLE
Storage
Shelf Life2 YEARS
Pack Size90 CAPSULES/BOTTLE
Dispensing Category
ATC Classification
Pharmaceutical Class
IndicationsFOR THE TREATMENT OF ADULT PATIENTS WHO HAVE RELAPSED OR REFRACTORY ACUTE MYELOID LEUKEMIA WITH AN FMS-LIKE TYROSINE KINASE 3 MUTATION
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionYELLOW PLAT TABLETS
Note
License OwnerLAOS ALLIANCE PHARMACEUTICAL GROUP COMPANY
ManufacturerLAOS ALLIANCE PHARMACEUTICAL GROUP COMPANY
CountryLAOS
Import Registration No
Import Registration Date
ActivityCERTIFICATE RELEASED
Applied Date
FDD Registration No11 L 1234/24
FDD Registration Date14/11/2024
Expiry Date13/11/2029
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