View the DEFERASIROX GPO registration information details.
Back to drug list
ItemsDrug Registration information
ID1106
No1106
Brand NameDEFERASIROX GPO
IngredientsDEFERASIROX 250 MG
Dosage FormDISPERSIBLE TABLET
Primary PackagingNYLON/ALU/PVC BLISTER
Storage
Shelf Life2 YEARS
Pack SizeBOX OF 3 X 10'S
Dispensing Category
ATC Classification
Pharmaceutical Class
IndicationsTREATMENT OF CHRONIC IRON OVERLOAD DUE TO BLOOD TRANSFUSIONS IN ADULT AND PEDIATRIC PATIENTS (AGED 2 YEARS AND OVER). ALSO INDICATED FOR THE TREATMENT OF CHRONIC IRON OVERLOAD IN PATIENTS WITH NONTRANSFUSION-DEPENDENT THALASSEMIA SYNDROMS AGED 10 YEARS AND OLDER
Contraindications
Side Effects
Unit Price
EDLNULL
DescriptionOFF WHITE, FLATE, ROUND, COMPRESSED TABLETS, ONE SIDE DEBOSEED WITH "D250" AND THE OTHER SIDE DEBOSSED WITH "GPO"
Note
License OwnerKARNYA VIENGNAKORN EXPORT-IMPORT
ManufacturerTHE GOVERNMENT PHARMACEUTICAL ORGANISATION
CountryTHAILAND
Import Registration No
Import Registration Date
ActivityCERTIFICATE RELEASED
Applied Date
FDD Registration No12 I 5163/21
FDD Registration Date10/09/2024
Expiry Date09/09/2029
Back to drug list
ADB ASEAN COVID-19 Laos JICA KOICA Global Fund WFP UHS Laos World Bank MOH Laos UNODC WHO SIDA