欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/1805/001
药品名称EPOPROSTENOL PH&T 0,5 mg, powder and solvent for solution for infusion
活性成分
    • epoprostenol sodium salt 0.5 mg
剂型Powder and solvent for solution for infusion
上市许可持有人PH&T S.p.A. Via L. Ariosto 34 20145 Milano Italy
参考成员国 - 产品名称Netherlands (NL)
Epoprostenol PH&T 0,5 mg, poeder en oplosmiddel voor oplossing voor infusie
互认成员国 - 产品名称
    许可日期2010/10/05
    最近更新日期2019/04/08
    药物ATC编码
      • B01AC09 epoprostenol
    申请类型
    • TypeLevel1:Known Active Substance
    • TypeLevel2:Initial Application
    • TypeLevel3:Bibliographic Art 10 a Dir 2001/83/EC
    • TypeLevel4:Chemical Substance
    • TypeLevel5:Prescription Only
    附件文件下载
    市场状态Withdrawn(注:已撤市)
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