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
Comtan Human entacapone entacapone EMEA/H/C/000171 Orion Corporation 1998/09/22 Authorised
Zartra Human imiquimod imiquimod EMEA/H/C/000180 Laboratoires 3M Santé 1998/09/18 Withdrawn
Aldara Human imiquimod imiquimod EMEA/H/C/000179 Viatris Healthcare Limited 1998/09/18 Authorised
Comtess Human entacapone entacapone EMEA/H/C/000170 Orion Corporation 1998/09/16 Authorised
Patrex Human sildenafil sildenafil EMEA/H/C/000204 Pfizer Limited 1998/09/15 Withdrawn
Viagra Human sildenafil sildenafil EMEA/H/C/000202 Upjohn EESV 1998/09/13 Authorised
Fortovase Human saquinavir saquinavir EMEA/H/C/000178 Roche Registration Ltd. 1998/08/20 Withdrawn
NovoNorm Human repaglinide repaglinide EMEA/H/C/000187 Novo Nordisk A/S 1998/08/16 Authorised
Evista Human raloxifene raloxifene hydrochloride EMEA/H/C/000184 Substipharm 1998/08/05 Authorised
Optruma Human raloxifene raloxifene hydrochloride EMEA/H/C/000185 Eli Lilly Nederland B.V. 1998/08/05 Authorised
Xenical Human orlistat orlistat EMEA/H/C/000154 CHEPLAPHARM Arzneimittel GmbH 1998/07/29 Authorised
EchoGen Human dodecafluoropentane dodecafluoropentane EMEA/H/C/000149 Sonus Pharmaceuticals Ltd. 1998/07/17 Withdrawn
Plavix Human clopidogrel clopidogrel hydrogen sulfate EMEA/H/C/000174 Sanofi Winthrop Industrie 1998/07/15 Authorised
Iscover Human clopidogrel clopidogrel EMEA/H/C/000175 Sanofi Winthrop Industrie 1998/07/14 Authorised
Turvel Human trovafloxacin trovafloxacin EMEA/H/C/000158 Pfizer Limited 1998/07/08 Withdrawn
Turvel IV Human trovafloxacin alatrofloxacin mesilate EMEA/H/C/000159 Pfizer Limited 1998/07/03 Withdrawn
Trovan IV Human trovafloxacin alatrofloxacin mesilate EMEA/H/C/000161 Pfizer Limited 1998/07/03 Withdrawn
Trovan Human trovafloxacin trovafloxacin EMEA/H/C/000160 Pfizer Limited 1998/07/03 Withdrawn
Pylori-Chek Human 13C-urea urea (13C) EMEA/H/C/000182 Alimenterics B.V. 1998/06/15 Withdrawn
MabThera Human rituximab rituximab EMEA/H/C/000165 Roche Registration GmbH 1998/06/02 Authorised

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