EPORATIO

This brand name is authorized in Austria, Croatia, Cyprus, Estonia, Finland, France, Germany, Ireland, Lithuania, Poland, Spain.

Active ingredients

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

1	Epoetin theta UNII 64FS3BFH5W - EPOETIN
	Epoetin theta is identical in its amino acid sequence and similar in its carbohydrate composition (glycosylation) to endogenous human erythropoietin. After administration of epoetin theta, the number of erythrocytes, the haematocrit values and reticulocyte counts increase.
	Read more about Epoetin theta

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
EPORATIO 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
B03XA01	Erythropoietin	B Blood and blood forming organs → B03 Antianemic preparations → B03X Other antianemic preparations → B03XA Other antianemic preparations
Discover more medicines within B03XA01

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	12411777, 12411783, 12411808, 12411814, 12411820, 12411837, 12411843, 12411866, 16808098, 17522961, 17522978, 17526551, 17570109
EE	Ravimiamet	1449985, 1449996, 1450000, 1450011, 1450022, 1450033, 1450044, 1450055, 1450066, 1450077, 1450088, 1450099, 1450101, 1450112, 1451292, 1451652, 1451720, 1451731, 1451742, 1451753, 1451764, 1451775, 1451786, 1451797, 1451809, 1451810, 1451821, 1451832
ES	Centro de información online de medicamentos de la AEMPS	109573037, 109573040
FI	Lääkealan turvallisuus- ja kehittämiskeskus	078520, 078531, 078544, 078555, 078566, 078577, 078588, 078599, 078610, 078621, 078633, 078644, 078655, 078666, 078677, 145689, 195918, 391030, 416665, 424098, 478005, 547303
FR	Base de données publique des médicaments	63088647, 65083079
IE	Health Products Regulatory Authority	88474, 88475, 88476, 88477, 88478, 88479, 88480, 88482
LT	Valstybinė vaistų kontrolės tarnyba	1051530, 1051531, 1051532, 1051533, 1051534, 1051535, 1051536, 1051537, 1051538, 1051539, 1051540, 1051541, 1051542, 1051543, 1051544, 1051545, 1051546, 1051547, 1051548, 1051549, 1051550, 1051551, 1051552, 1051553, 1051554, 1051555, 1051556, 1051557, 1078881, 1078882, 1078883, 1078884, 1078887, 1078888, 1078889, 1078890, 1078891, 1078892, 1078893, 1078894, 1078895, 1078896
PL	Rejestru Produktów Leczniczych	100236604, 100236610, 100236627, 100236633, 100236640, 100236656, 100236662, 100236679