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
Pemetrexed Baxter Human pemetrexed pemetrexed disodium heptahydrate EMEA/H/C/005848 Baxter Holding B.V. 2022/12/09 Authorised
Pemetrexed Krka Human pemetrexed pemetrexed disodium EMEA/H/C/003958 KRKA d.d. 2018/05/22 Withdrawn
Pemetrexed Pfizer (previously Pemetrexed Hospira UK Limited) Human pemetrexed pemetrexed ditromethamine EMEA/H/C/004488 Pfizer Europe MA EEIG 2017/04/24 Withdrawn
Pemetrexed Fresenius Kabi Human pemetrexed pemetrexed EMEA/H/C/003895 Fresenius Kabi Deutschland GmbH 2016/07/22 Authorised
Pemetrexed Accord Human pemetrexed pemetrexed disodium hemipentahydrate EMEA/H/C/004072 Accord Healthcare S.L.U. 2016/01/18 Authorised
Armisarte (previously Pemetrexed Actavis) Human pemetrexed pemetrexed diacid monohydrate EMEA/H/C/004109 Actavis Group PTC ehf 2016/01/18 Authorised
Ciambra Human pemetrexed pemetrexed disodium hemipentahydrate EMEA/H/C/003788 Menarini International Operations Luxembourg S.A. 2015/12/02 Withdrawn
Pemetrexed medac Human pemetrexed pemetrexed EMEA/H/C/003905 medac Gesellschaft für klinische Spezialpräparate mbH 2015/11/26 Authorised
Pemetrexed Pfizer (previously Pemetrexed Hospira) Human pemetrexed pemetrexed disodium;pemetrexed disodium hemipentahydrate EMEA/H/C/003970 Pfizer Europe MA EEIG 2015/11/19 Authorised
Pemetrexed Sandoz Human pemetrexed pemetrexed disodium hemipentahydrate EMEA/H/C/004011 Sandoz GmbH 2015/09/18 Withdrawn
Pemetrexed Lilly Human pemetrexed pemetrexed EMEA/H/C/004114 Eli Lilly Netherlands 2015/09/14 Withdrawn
Alimta Human pemetrexed pemetrexed EMEA/H/C/000564 Eli Lilly Nederland B.V. 2004/09/20 Authorised
Pemetrexed ditromethamine Hospira Human pemetrexed pemetrexed ditromethamine EMEA/H/C/004306 Application withdrawn

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