IDELVION

This brand name is authorized in Austria, Brazil, Canada, Croatia, Cyprus, Estonia, France, Hong Kong SAR China, Ireland, Israel, Italy, Japan, Lithuania, Netherlands, New Zealand, Poland, Singapore, Spain, Turkey, UK.

Active ingredients

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

1	Coagulation factor IX UNII A57KX1VL5P - ALBUTREPENONACOG ALFA
	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	502619030008507, 502619030008607, 502619030008707, 502619030008807
CA	Health Products and Food Branch	02451352
EE	Ravimiamet	1718625, 1718636, 1718647, 1718658, 1826119
ES	Centro de información online de medicamentos de la AEMPS	1161095001, 1161095002, 1161095003, 1161095004
FR	Base de données publique des médicaments	60216127, 63102506, 65247870
GB	Medicines & Healthcare Products Regulatory Agency	328156, 328160, 328188, 328194
HK	Department of Health Drug Office	65142, 65143, 65144, 65145
IL	מִשְׂרַד הַבְּרִיאוּת	8411, 8412, 8413
IT	Agenzia del Farmaco	044891012, 044891024, 044891036, 044891048, 044891051
JP	医薬品医療機器総合機構	6343448D1020, 6343448D2026, 6343448D3022, 6343448D4029, 6343448D5025
LT	Valstybinė vaistų kontrolės tarnyba	1080374, 1080375, 1080376, 1080377, 1091048
NL	Z-Index G-Standaard	14281910, 14281929, 14281937
NL	Z-Index G-Standaard, PRK	132365, 132373, 132403, 132500
NZ	Medicines and Medical Devices Safety Authority	18603, 18604, 18605, 18606, 22393
PL	Rejestru Produktów Leczniczych	100372514, 100372520, 100372773, 100372796, 100461213
SG	Health Sciences Authority	15811P, 15812P, 15813P, 15814P
TR	İlaç ve Tıbbi Cihaz Kurumu	8681624980330, 8681624980347, 8681624980354, 8681624980361