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 14 条，共 1 页，当前第 1 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
Eporatio Human epoetin theta epoetin theta EMEA/H/C/001033 Ratiopharm GmbH 2009/10/29 Authorised
Biopoin Human epoetin theta epoetin theta EMEA/H/C/001036 Teva GmbH 2009/10/23 Authorised
Retacrit Human epoetin zeta epoetin zeta EMEA/H/C/000872 Pfizer Europe MA EEIG 2007/12/18 Authorised
Silapo Human epoetin zeta epoetin zeta EMEA/H/C/000760 Stada Arzneimittel AG 2007/12/18 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
Mircera Human methoxy polyethylene glycol-epoetin beta Methoxy polyethylene glycol-epoetin beta EMEA/H/C/000739 Roche Registration GmbH 2007/07/20 Authorised
Dynepo Human epoetin delta epoetin delta EMEA/H/C/000372 Shire Pharmaceutical Contracts Limited 2002/03/18 Withdrawn
Aranesp Human darbepoetin alfa darbepoetin alfa EMEA/H/C/000332 Amgen Europe B.V. 2001/06/08 Authorised
Nespo Human darbepoetin alfa darbepoetin alfa EMEA/H/C/000333 Dompé Biotec S.p.A. 2001/06/08 Withdrawn
NeoRecormon Human epoetin beta epoetin beta EMEA/H/C/000116 Roche Registration GmbH 1997/07/16 Authorised
Epostim Human epoetin alfa epoetin alfa EMEA/H/C/002265 Reliance GeneMedix Plc Application withdrawn
Ratioepo Human epoetin theta epoetin theta EMEA/H/C/001035 Ratiopharm GmbH Application withdrawn

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