ELOCTA

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, Finland, France, Ireland, Israel, Lithuania, Netherlands, Poland, Romania, Spain, Tunisia, Turkey, UK.

Active ingredients

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

1	Efmoroctocog alfa UNII 839MOZ74GK - ANTIHEMOPHILIC FACTOR HUMAN
	Activated factor VIII acts as a cofactor for activated factor IX, accelerating the conversion of factor X to activated factor X (factor Xa). Haemophilia A is a sex-linked hereditary disorder of blood coagulation due to decreased levels of factor VIII:C. By replacement therapy the plasma levels of factor VIII are increased, thereby enabling a temporary correction of the factor deficiency and correction of the bleeding tendencies.
	Read more about Coagulation factor VIII

Medicine classification

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

ATC Group		Classification
B02BD02	Coagulation factor VIII	B Blood and blood forming organs → B02 Antihemorrhagics → B02B Vitamin K and other hemostatics → B02BD Blood coagulation factors
Discover more medicines within B02BD02

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
EE	Ravimiamet	1704237, 1704248, 1704259, 1704260, 1704271, 1704282, 1704293, 1786495, 1786507, 1786518
ES	Centro de información online de medicamentos de la AEMPS	1151046001, 1151046002, 1151046003, 1151046004, 1151046005, 1151046006, 1151046007, 1151046008
FI	Lääkealan turvallisuus- ja kehittämiskeskus	071580, 183310, 183367, 396284, 403970, 422661, 479988, 557760
FR	Base de données publique des médicaments	60602449, 63314092, 63964656, 64440763, 66735584, 68853909, 69009069, 69349794
GB	Medicines & Healthcare Products Regulatory Agency	310722, 310723, 310724, 310725, 310726, 310727, 332572, 379769
IL	מִשְׂרַד הַבְּרִיאוּת	9069, 9070, 9071
LT	Valstybinė vaistų kontrolės tarnyba	1078859, 1078860, 1078863, 1078864, 1078865, 1078866, 1078867, 1086904, 1086905, 1086906
NL	Z-Index G-Standaard	14266458, 14266466, 14266474, 14816466
NL	Z-Index G-Standaard, PRK	129291, 129305, 129313, 129321, 129348, 129356, 129364, 201162
PL	Rejestru Produktów Leczniczych	100357130, 100357331, 100357348, 100357354, 100357360, 100357377, 100357383, 100417493, 100417501, 100417518
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W62680001, W62681001, W62682001, W62683001, W62684001, W62685001, W62686001
TN	Direction de la Pharmacie et du Médicament	16673021H, 16673022H
TR	İlaç ve Tıbbi Cihaz Kurumu	8683125910014, 8683125910021, 8683125910038, 8683125910045, 8683125910052, 8683125910069