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 2640 条，共 132 页，当前第 94 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
Cetrotide Human cetrorelix cetrorelix (as acetate) EMEA/H/C/000233 Merck Europe B.V. 1999/04/12 Authorised
Beromun Human tasonermin tasonermin EMEA/H/C/000206 Belpharma s.a. 1999/04/12 Authorised
Regranex Human becaplermin becaplermin EMEA/H/C/000212 Janssen-Cilag International NV 1999/03/29 Withdrawn
Sonata Human zaleplon zaleplon EMEA/H/C/000227 Meda AB 1999/03/12 Withdrawn
Zerene Human zaleplon zaleplon EMEA/H/C/000228 Meda AB 1999/03/12 Withdrawn
Zenapax Human daclizumab daclizumab EMEA/H/C/000198 Roche Registration Ltd. 1999/02/26 Withdrawn
Infergen Human interferon alfacon-1 interferon alfacon-1 EMEA/H/C/000186 Astellas Pharma Europe B.V. 1999/02/01 Withdrawn
Emadine Human emedastine emedastine difumarate EMEA/H/C/000223 Immedica Pharma AB 1999/01/27 Authorised
Temodal Human temozolomide temozolomide EMEA/H/C/000229 Merck Sharp & Dohme B.V.  1999/01/26 Authorised
Forcaltonin Human recombinant salmon calcitonin recombinant salmon calcitonin EMEA/H/C/000197 Unigene UK Ltd. 1999/01/11 Withdrawn
Triacelluvax Human diphtheria, tetanus and pertussis (acellular, component) vaccine (adsorbed) Diphtheria toxoid;haemagglutinin filamentous;pertussis pertactin;pertussis toxin;tetanus toxoid EMEA/H/C/000181 Chiron S.p.A. 1999/01/11 Withdrawn
Micardis Human telmisartan telmisartan EMEA/H/C/000209 Boehringer Ingelheim International GmbH 1998/12/16 Authorised
Kinzalmono (previously Telmisartan Boehringer Ingelheim Pharma KG) Human telmisartan telmisartan EMEA/H/C/000211 Bayer AG 1998/12/16 Authorised
Pritor Human telmisartan telmisartan EMEA/H/C/000210 Bayer AG 1998/12/11 Authorised
Prometax Human rivastigmine rivastigmine EMEA/H/C/000255 Almirall, S.A. 1998/12/04 Authorised
Karvezide Human irbesartan;hydrochlorothiazide irbesartan;hydrochlorothiazide EMEA/H/C/000221 Sanofi Winthrop Industrie 1998/10/16 Authorised
CoAprovel Human irbesartan;hydrochlorothiazide irbesartan;hydrochlorothiazide EMEA/H/C/000222 Sanofi Winthrop Industrie 1998/10/14 Authorised
Simulect Human basiliximab basiliximab EMEA/H/C/000207 Novartis Europharm Limited 1998/10/09 Authorised
HumaSPECT Human votumumab votumumab EMEA/H/C/000145 KS Biomedix Limited 1998/09/25 Withdrawn
Comtan Human entacapone entacapone EMEA/H/C/000171 Orion Corporation 1998/09/22 Authorised

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