欧盟EMA药品数据库-欧盟集中审批药品
(European Medicines Agency Authorisation of Medicines DataBase)
商品名称 适用类别 通用名称 活性成分 产品号 上市许可开发者/申请人/持有人 上市许可日期 许可状态
Trisenox Human arsenic trioxide arsenic trioxide EMEA/H/C/000388 Teva B.V. 2002/03/05 Authorised
Protopy Human tacrolimus tacrolimus EMEA/H/C/000375 Astellas Pharma GmbH 2002/02/28 Withdrawn
Protopic Human tacrolimus tacrolimus EMEA/H/C/000374 LEO Pharma A/S 2002/02/27 Authorised
Viread Human tenofovir disoproxil tenofovir disoproxil fumarate EMEA/H/C/000419 Gilead Sciences Ireland UC 2002/02/04 Authorised
Travatan Human travoprost travoprost EMEA/H/C/000390 Novartis Europharm Limited 2001/11/27 Authorised
Glivec Human imatinib imatinib EMEA/H/C/000406 Novartis Europharm Limited 2001/11/07 Authorised
Foscan Human temoporfin temoporfin EMEA/H/C/000318 Biolitec Pharma Ltd 2001/10/24 Authorised
Cancidas (previously Caspofungin MSD) Human caspofungin caspofungin (as acetate) EMEA/H/C/000379 2001/10/23 Authorised
Replagal Human agalsidase alfa agalsidase alfa EMEA/H/C/000369 Takeda Pharmaceuticals International AG Ireland Branch 2001/08/03 Authorised
Fabrazyme Human agalsidase beta agalsidase beta EMEA/H/C/000370 Sanofi B.V. 2001/08/03 Authorised
INOmax Human nitric oxide nitric oxide EMEA/H/C/000337 Linde Healthcare AB 2001/08/01 Authorised
Liprolog Human insulin lispro insulin lispro EMEA/H/C/000393 Eli Lilly Nederland B.V. 2001/08/01 Authorised
Ceprotin Human human protein C human protein C EMEA/H/C/000334 Takeda Manufacturing Austria AG 2001/07/16 Authorised
DepoCyte Human cytarabine cytarabine EMEA/H/C/000317 Pacira Limited 2001/07/11 Withdrawn
Ketek Human telithromycin telithromycin EMEA/H/C/000354 Aventis Pharma S.A. 2001/07/09 Withdrawn
Levviax Human telithromycin telithromycin EMEA/H/C/000355 Aventis Pharma S.A. 2001/07/09 Withdrawn
MabCampath Human alemtuzumab alemtuzumab EMEA/H/C/000353 Genzyme Europe B.V. 2001/07/06 Withdrawn
Nonafact Human human coagulation factor IX human coagulation factor IX EMEA/H/C/000348 Sanquin Plasma Products B.V. 2001/07/03 Withdrawn
Aranesp Human darbepoetin alfa darbepoetin alfa EMEA/H/C/000332 Amgen Europe B.V. 2001/06/08 Authorised
Nespo Human darbepoetin alfa darbepoetin alfa EMEA/H/C/000333 Dompé Biotec S.p.A. 2001/06/08 Withdrawn

数据库说明:

©2006-2026 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase