IMUKIN

This brand name is authorized in Australia, Austria, Estonia, France, Malta, Spain.

Active ingredients

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

1
UNII 21K6M2I7AG - INTERFERON GAMMA-1B
 

It is presumed that interferon gamma-1b increases macrophage cytotoxicity by enhancing the respiratory burst via generation of toxic oxygen metabolites capable of mediating the killing of intracellular micro-organisms.

 
Read more about Interferon gamma-1b

Medicine classification

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

ATC Group Classification
L03AB03 Interferon gamma L Antineoplastic and immunomodulating agents → L03 Immunostimulants → L03A Immunostimulants → L03AB Interferons
Discover more medicines within L03AB03

Authorization and marketing

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

Country Identification scheme Identifier(s)
AU Pharmaceutical Benefits Scheme 5769P, 6148N
EE Ravimiamet 1681332, 1708657
ES Centro de información online de medicamentos de la AEMPS 60113
FR Base de données publique des médicaments 67401121
MT Medicines Authority AA565/39303

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