欧盟EMA药品数据库-欧盟集中审批药品
（European Medicines Agency Authorisation of Medicines DataBase）
请输入需要查询的英文药品名称，通用名称，活性成分，产品号
*Search by Medicine name,INN,Active substance,Product number.
高级搜索
数据记录共 2649 条，共 133 页，当前第 78 页
可点击列名称排序
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
Enviage Human aliskiren aliskiren EMEA/H/C/000850 Novartis Europharm Ltd. 2007/08/22 Withdrawn
Tekturna Human aliskiren aliskiren EMEA/H/C/000852 Novartis Europharm Ltd. 2007/08/22 Withdrawn
Increlex Human mecasermin Mecasermin EMEA/H/C/000704 Esteve Pharmaceuticals, S.A. 2007/08/02 Authorised
Aerinaze Human desloratadine;pseudoephedrine desloratadine;pseudophedrine sulfate EMEA/H/C/000772 N.V. Organon 2007/07/30 Authorised
Flebogamma DIF (previously Flebogammadif) Human human normal immunoglobulin human normal immunoglobulin EMEA/H/C/000781 Instituto Grifols S.A. 2007/07/23 Authorised
Optimark Human gadoversetamide gadoversetamide EMEA/H/C/000745 Mallinckrodt Deutschland GmbH 2007/07/23 Withdrawn
Alli (previously Orlistat GSK) Human orlistat orlistat EMEA/H/C/000854 Haleon Ireland Dungarvan Limited 2007/07/22 Authorised
Mircera Human methoxy polyethylene glycol-epoetin beta Methoxy polyethylene glycol-epoetin beta EMEA/H/C/000739 Roche Registration GmbH 2007/07/20 Authorised
Siklos Human hydroxycarbamide hydroxycarbamide EMEA/H/C/000689 Theravia 2007/06/29 Authorised
Circadin Human melatonin melatonin EMEA/H/C/000695 RAD Neurim Pharmaceuticals EEC SARL 2007/06/29 Authorised
Pergoveris Human follitropin alfa;lutropin alfa follitropin alfa;lutropin alfa EMEA/H/C/000714 Merck Europe B.V.  2007/06/25 Authorised
Invega Human paliperidone paliperidone EMEA/H/C/000746 Janssen-Cilag International NV 2007/06/24 Authorised
Soliris Human eculizumab Eculizumab EMEA/H/C/000791 2007/06/20 Authorised
Spironolactone Ceva Veterinary spironolactone spironolactone EMEA/V/C/000105 Ceva Santé Animale 2007/06/20 Withdrawn
Revlimid Human lenalidomide lenalidomide EMEA/H/C/000717 Bristol-Myers Squibb Pharma EEIG 2007/06/14 Authorised
Optaflu Human influenza vaccine (surface antigen, inactivated, prepared in cell cultures) influenza virus surface antigens (haemagglutinin and neuraminidase), inactivated, of the following strains:A/California/7/2009 (H1N1)pdm09 - like strain(A/Brisbane/10/2010, wild type)A/Switzerland/9715293/2013 (H3N2) - like strain(A/South Australia/55/2014, wild type)B/Phuket/3073/2013–like strain(B/Utah/9/2014, wild type) EMEA/H/C/000758 Seqirus GmbH 2007/06/01 Expired
Altargo Human retapamulin retapamulin EMEA/H/C/000757 Glaxo Group Ltd 2007/05/24 Withdrawn
Orencia Human abatacept abatacept EMEA/H/C/000701 Bristol-Myers Squibb Pharma EEIG 2007/05/21 Authorised
Nobilis Influenza H7N1 Veterinary adjuvanted inactivated vaccine against avian influenza virus type A, subtype H7 inactivated whole avian influenza virus antigen of H7N1 subtype (strain, A/CK/Italy/473/99) EMEA/V/C/000123 Intervet International BV 2007/05/14 Withdrawn
Focetria Human influenza vaccine H1N1v (surface antigen, inactivated, adjuvanted) Influenza virus surface antigens (haemagglutinin and neuraminidase) of strain: A/California/7/2009 (H1N1)-derived strain used NYMC X-181 EMEA/H/C/000710 Novartis Vaccines and Diagnostics S.r.l. 2007/05/02 Expired

数据库说明：

©2006-2025 DrugFuture->European Medicines Agency Authorisation of Medicines DataBase