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.
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数据记录共 2655 条，共 133 页，当前第 78 页
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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
Galvus Human vildagliptin vildagliptin EMEA/H/C/000771 Novartis Europharm Limited 2007/09/25 Authorised
Ecalta Human anidulafungin anidulafungin EMEA/H/C/000788 Pfizer Europe MA EEIG 2007/09/20 Authorised
Cervarix Human human papillomavirus vaccine [types 16, 18] (recombinant, adjuvanted, adsorbed) human papillomavirus1 type 16 L1 protein;human papillomavirus type 18 L1 protein EMEA/H/C/000721 GlaxoSmithKline Biologicals S.A. 2007/09/20 Authorised
Celsentri Human maraviroc maraviroc EMEA/H/C/000811 ViiV Healthcare B.V. 2007/09/18 Authorised
Yondelis Human trabectedin trabectedin EMEA/H/C/000773 Pharma Mar S.A. 2007/09/17 Authorised
Gliolan Human 5-aminolevulinic acid hydrochloride 5-aminolevulinic acid hydrochloride EMEA/H/C/000744 Photonamic GmbH & Co. KG 2007/09/07 Authorised
Binocrit Human epoetin alfa epoetin alfa EMEA/H/C/000725 Sandoz GmbH 2007/08/28 Authorised
Epoetin Alfa Hexal Human epoetin alfa epoetin alfa EMEA/H/C/000726 Hexal AG 2007/08/27 Authorised
Abseamed Human epoetin alfa epoetin alfa EMEA/H/C/000727 Medice Arzneimittel Pütter GmbH Co. KG 2007/08/27 Authorised
Atriance Human nelarabine nelarabine EMEA/H/C/000752 Sandoz Pharmaceuticals d.d. 2007/08/22 Authorised
Rasilez Human aliskiren aliskiren EMEA/H/C/000780 Noden Pharma DAC 2007/08/22 Authorised
Riprazo Human aliskiren aliskiren EMEA/H/C/000853 Novartis Europharm Ltd. 2007/08/22 Withdrawn
Sprimeo Human aliskiren aliskiren EMEA/H/C/000851 Novartis Europharm Ltd. 2007/08/22 Withdrawn
Enviage Human aliskiren aliskiren EMEA/H/C/000850 Novartis Europharm Ltd. 2007/08/22 Withdrawn
Tekturna Human aliskiren aliskiren EMEA/H/C/000852 Novartis Europharm Ltd. 2007/08/22 Withdrawn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

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