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
Pregabalin Mylan Pharma Human pregabalin pregabalin EMEA/H/C/003962 Mylan S.A.S. 2015/06/25 Withdrawn
Pregabalin Viatris (previously Pregabalin Mylan) Human pregabalin pregabalin EMEA/H/C/004078 Viatris Limited 2015/06/24 Authorised
Opdivo Human nivolumab nivolumab EMEA/H/C/003985 Bristol-Myers Squibb Pharma EEIG 2015/06/19 Authorised
Pregabalin Sandoz Human pregabalin pregabalin EMEA/H/C/004010 Sandoz GmbH 2015/06/19 Authorised
Duloxetine Viatris (previously Duloxetine Mylan) Human duloxetine duloxetine EMEA/H/C/003981 Viatris Limited 2015/06/19 Authorised
Lixiana Human edoxaban edoxaban tosilate EMEA/H/C/002629 Daiichi Sankyo Europe GmbH 2015/06/19 Authorised
Pregabalin Sandoz GmbH Human pregabalin pregabalin EMEA/H/C/004070 Sandoz GmbH 2015/06/19 Withdrawn
Lumark Human lutetium (177Lu) chloride lutetium (177Lu) chloride EMEA/H/C/002749 I.D.B. Radiopharmacy B.V. 2015/06/18 Withdrawn
Gardasil 9 Human human papillomavirus 9-valent vaccine (recombinant, adsorbed) human papillomavirus vaccine [types 6, 11, 16, 18, 31, 33, 45, 52, 58] (recombinant, adsorbed) EMEA/H/C/003852 Merck Sharp & Dohme B.V. 2015/06/10 Authorised
Lenvima Human lenvatinib lenvatinib mesilate EMEA/H/C/003727 Eisai GmbH 2015/05/28 Authorised
Akynzeo Human netupitant;palonosetron netupitant;palonosetron hydrochloride EMEA/H/C/003728 Helsinn Birex Pharmaceuticals Ltd 2015/05/27 Authorised
Voriconazole Hikma (previously Voriconazole Hospira) Human voriconazole voriconazole EMEA/H/C/003737 Hikma Farmaceutica (Portugal) S.A. 2015/05/27 Authorised
Synjardy Human empagliflozin;metformin empagliflozin;metformin EMEA/H/C/003770 Boehringer Ingelheim 2015/05/27 Authorised
Jinarc Human tolvaptan tolvaptan EMEA/H/C/002788 Otsuka Pharmaceutical Netherlands B.V. 2015/05/27 Authorised
Zykadia Human ceritinib ceritinib EMEA/H/C/003819 Novartis Europharm Limited 2015/05/06 Authorised
Ristempa Human pegfilgrastim pegfilgrastim EMEA/H/C/003910 Amgen Europe B.V. 2015/04/13 Withdrawn
Mysimba Human naltrexone;bupropion bupropion hydrochloride;naltrexone hydrochloride EMEA/H/C/003687 Orexigen Therapeutics Ireland Limited 2015/03/26 Authorised
Dutrebis Human lamivudine;raltegravir potassium lamivudine;raltegravir potassium EMEA/H/C/003823 Merck Sharp Dohme Limited 2015/03/26 Withdrawn
Quinsair Human levofloxacin levofloxacin EMEA/H/C/002789 Chiesi Farmaceutici S.p.A 2015/03/25 Authorised
Kengrexal Human cangrelor cangrelor EMEA/H/C/003773 Chiesi Farmaceutici S.p.A. 2015/03/23 Authorised

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