LEUKOSCAN

This brand name is authorized in Lithuania, Spain.

Active ingredients

The drug LEUKOSCAN contains one active pharmaceutical ingredient (API):

1
UNII 0G1945O6IB - SULESOMAB TECHNETIUM TC-99M
 

Technetium ⁹⁹ᵐTc sulesomab (IMMU-MN3 murine Fab′-SH antigranulocyte monoclonal antibody fragments) recognizes an antigenic structure shared by a surface glycoprotein (NCA-90) of granulocytes and the tumour marker. It is indicated for diagnostic imaging for determining the location and extent of infection/inflammation in bone in patients with suspected osteomyelitis, including patients with diabetic foot ulcers.

 
Read more about Technetium ⁹⁹ᵐTc sulesomab

Medication package inserts

Below package inserts are available for further reading:

Document Type Information Source  
 LEUKOSCAN Powder for solution for injection MPI, EU: SmPC European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group Classification
V09HA04 Technetium (99mTc) sulesomab V Various → V09 Diagnostic radiopharmaceuticals → V09H Inflammation and infection detection → V09HA Technetium (99mTc) compounds
Discover more medicines within V09HA04

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country Identification scheme Identifier(s)
ES Centro de información online de medicamentos de la AEMPS 98032001
LT Valstybinė vaistų kontrolės tarnyba 1029389

© All content on this website, including data entry, data processing, decision support tools, "RxReasoner" logo and graphics, is the intellectual property of RxReasoner and is protected by copyright laws. Unauthorized reproduction or distribution of any part of this content without explicit written permission from RxReasoner is strictly prohibited. Any third-party content used on this site is acknowledged and utilized under fair use principles.