RIXUBIS

This brand name is authorized in Austria, Brazil, Canada, Croatia, Estonia, Finland, France, Ireland, Italy, Lithuania, Netherlands, New Zealand, Poland, Spain, Turkey, UK.

Active ingredients

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

1
UNII 382L14738L - COAGULATION FACTOR IX RECOMBINANT HUMAN
 

Factor IX is a single chain glycoprotein with a molecular mass of about 68,000 Dalton. It is a vitamin-K dependent coagulation factor and it is synthesised in the liver. Factor IX is activated by factor XIa in the intrinsic coagulation pathway and by the factor VII/tissue factor complex in the extrinsic pathway. Activated factor IX, in combination with activated factor VIII, activates factor X.

 
Read more about Coagulation factor IX

Medicine classification

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

ATC Group Classification
B02BD04 Coagulation factor IX B Blood and blood forming organs → B02 Antihemorrhagics → B02B Vitamin K and other hemostatics → B02BD Blood coagulation factors
Discover more medicines within B02BD04

Authorization and marketing

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

Country Identification scheme Identifier(s)
BR Câmara de Regulação do Mercado de Medicamentos 501121010033217, 501121010033317, 501121010033417, 501121010033517
CA Health Products and Food Branch 02431920, 02431939, 02431947, 02431955, 02431963
EE Ravimiamet 1674165, 1674176, 1674187, 1674198, 1674200
ES Centro de información online de medicamentos de la AEMPS 114970001, 114970002, 114970003, 114970004, 114970005
FI Lääkealan turvallisuus- ja kehittämiskeskus 076982, 090653, 096576, 522610, 590608
FR Base de données publique des médicaments 60287206, 60351694, 63756662, 65587061, 66329427
GB Medicines & Healthcare Products Regulatory Agency 326895, 326899, 326903, 326907, 326911
IT Agenzia del Farmaco 043796010, 043796022, 043796034, 043796046, 043796059
LT Valstybinė vaistų kontrolės tarnyba 1075441, 1075442, 1075443, 1075444, 1075445
NL Z-Index G-Standaard, PRK 129046, 129054, 129062, 129070, 129089
NZ Medicines and Medical Devices Safety Authority 15909, 15910, 15911, 15912, 15913
PL Rejestru Produktów Leczniczych 100335973, 100335980, 100335996, 100336004, 100336056
TR İlaç ve Tıbbi Cihaz Kurumu 8681429550585, 8681429550592, 8681429550608, 8681429550615, 8681429550622

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