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 16 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
Usgena Human ustekinumab ustekinumab EMEA/H/C/006667 Stada Arzneimittel AG 2025/11/17 Authorised
Usrenty Human ustekinumab ustekinumab EMEA/H/C/006794 Biosimilar Collaborations Ireland Limited 2025/09/17 Authorised
Usymro Human ustekinumab ustekinumab EMEA/H/C/006467 Gedeon Richter Plc. 2025/08/14 Authorised
Qoyvolma Human ustekinumab ustekinumab EMEA/H/C/006649 Celltrion Healthcare Hungary Kft. 2025/06/02 Authorised
Yesintek Human ustekinumab ustekinumab EMEA/H/C/006444 Biosimilar Collaborations Ireland Limited 2025/02/14 Authorised
Absimky Human ustekinumab ustekinumab EMEA/H/C/006585 Accord Healthcare S.L.U. 2024/12/12 Withdrawn
Imuldosa Human ustekinumab ustekinumab EMEA/H/C/006221 Accord Healthcare S.L.U. 2024/12/12 Authorised
Otulfi Human ustekinumab ustekinumab EMEA/H/C/006544 Fresenius Kabi Deutschland GmbH 2024/09/25 Authorised
Fymskina Human ustekinumab ustekinumab EMEA/H/C/005805 Formycon AG 2024/09/25 Authorised
Eksunbi Human ustekinumab ustekinumab EMEA/H/C/006448 Samsung Bioepis NL B.V. 2024/09/12 Withdrawn
Steqeyma Human ustekinumab ustekinumab EMEA/H/C/005918 Celltrion Healthcare Hungary Kft. 2024/08/22 Authorised
Wezenla Human ustekinumab ustekinumab EMEA/H/C/006132 Amgen Technology (Ireland) UC 2024/06/20 Authorised
Pyzchiva Human ustekinumab ustekinumab EMEA/H/C/006183 Samsung Bioepis NL B.V. 2024/04/19 Authorised
Uzpruvo Human ustekinumab ustekinumab EMEA/H/C/006101 Stada Arzneimittel AG 2024/01/05 Authorised
Stelara Human ustekinumab ustekinumab EMEA/H/C/000958 Janssen-Cilag International NV 2009/01/15 Authorised
Upstelda Human ustekinumab ustekinumab EMEA/H/C/006415 Amgen Technology (Ireland) UC Application withdrawn

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