欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）

MR编号	NL/H/3585/001
药品名称	Iloprost Solufarma 20 micrograms/1ml
活性成分	iloprost trometamine 20.0 µg/ml
剂型	Concentrate for solution for infusion
上市许可持有人	Pharmanovia A/S Copenhagen Towers Oerestads Boulevard 108, 5 Tv 2300 Denmark
参考成员国 - 产品名称	Netherlands (NL) Iloprost Solufarma 20 micrograms/1ml
互认成员国 - 产品名称	Denmark (DK) Iloprost Solufarma Germany (DE) Iloprost Waymade 20 µg/ml, Konzentrat zur Herstellung einer Infusionslösung Austria (AT) Sweden (SE)
许可日期	2017/05/03
最近更新日期	2024/01/29
药物ATC编码	B01AC11 iloprost
申请类型	TypeLevel1：Known Active Substance TypeLevel2：Initial Application TypeLevel3：Generic Art 10.1 and 10.2 Dir 2001/83/EC TypeLevel4：Chemical Substance TypeLevel5：Prescription Only
附件文件下载	Final PL \| common_pl_20_cleanDate of last change:2023/06/28 Final SPC \| common_spc_20_cleanDate of last change:2023/06/28 PAR Summary \| 171110 NL.H.3585.001-002.DC Iloprost Solufarma summary ENDate of last change:2017/11/29 PAR \| 171110 NL.H.3585.001-002.DC Iloprost Solufarma final PARDate of last change:2017/11/29 Final Labelling \| common-inner-label-100Date of last change:2017/05/04 Final Labelling \| common-inner-label-20Date of last change:2017/05/04 Final Labelling \| common-outer-label-100-May 17Date of last change:2017/05/04 Final Labelling \| common-outer-label-20-May 17Date of last change:2017/05/04
市场状态	Positive