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 2679 条，共 134 页，当前第 73 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
Clopidogrel DURA Human clopidogrel clopidogrel (as hydrochloride) EMEA/H/C/001132 Mylan dura GmbH 2009/07/21 Withdrawn
Instanyl Human fentanyl Fentanyl citrate EMEA/H/C/000959 Istituto Gentili S.r.l. 2009/07/20 Authorised
Peyona (previously Nymusa) Human caffeine Caffeine citrate EMEA/H/C/001014 Chiesi Farmaceutici SpA 2009/07/02 Authorised
Ribavirin Teva Pharma B.V. Human ribavirin ribavirin EMEA/H/C/001064 Teva B.V. 2009/07/01 Withdrawn
Victoza Human liraglutide liraglutide EMEA/H/C/001026 Novo Nordisk A/S 2009/06/30 Authorised
Repaglinide Teva Human repaglinide repaglinide EMEA/H/C/001067 Teva Pharma B.V. 2009/06/28 Authorised
Iressa Human gefitinib gefitinib EMEA/H/C/001016 AstraZeneca AB 2009/06/24 Authorised
Somac Control Human pantoprazole pantoprazole EMEA/H/C/001098 Takeda GmbH 2009/06/12 Authorised
Pantecta Control Human pantoprazole pantoprazole EMEA/H/C/001099 Takeda GmbH 2009/06/12 Withdrawn
Pantozol Control Human pantoprazole pantoprazole EMEA/H/C/001013 Takeda GmbH 2009/06/11 Authorised
Controloc Control Human pantoprazole pantoprazole EMEA/H/C/001097 Takeda GmbH 2009/06/11 Authorised
Pantoloc Control Human pantoprazole pantoprazole EMEA/H/C/001100 Takeda GmbH 2009/06/11 Withdrawn
Renvela Human sevelamer carbonate sevelamer carbonate EMEA/H/C/000993 Sanofi Winthrop Industrie 2009/06/09 Authorised
Qutenza Human capsaicin capsaicin EMEA/H/C/000909 Grunenthal GmbH 2009/05/15 Authorised
ellaOne Human ulipristal acetate ulipristal EMEA/H/C/001027 Laboratoire HRA Pharma 2009/05/15 Authorised
Modigraf Human tacrolimus tacrolimus EMEA/H/C/000954 Astellas Pharma Europe B.V. 2009/05/15 Authorised
Nimvastid Human rivastigmine rivastigmine EMEA/H/C/001029 Krka, d.d., Novo mesto 2009/05/11 Authorised
Zebinix Human eslicarbazepine acetate eslicarbazepine acetate EMEA/H/C/000988 BIAL - Portela & Ca, S.A. 2009/04/21 Authorised
Exalief Human eslicarbazepine acetate eslicarbazepine acetate EMEA/H/C/000987 BIAL - Portela Ca, S.A. 2009/04/21 Lapsed
Removab Human catumaxomab catumaxomab EMEA/H/C/000972 Neovii Biotech GmbH 2009/04/20 Withdrawn

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