欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/8013/001
药品名称Thiotepa Vivanta 15 mg Pulver für ein Konzentrat zur Herstellung einer Infusionslösung
活性成分
    • Thiotepa 15.0 mg
剂型Powder and solvent for concentrate for solution for infusion
上市许可持有人Vivanta Generics s.r.o. Trtinova 260/1 Cakovice 196 00 Prague-Cakovice Czechia
参考成员国 - 产品名称Germany (DE)
Thiotepa Vivanta 15 mg Pulver für ein Konzentrat zur Herstellung einer Infusionslösung
互认成员国 - 产品名称
    • Croatia (HR)
    • Poland (PL)
      Thiotepa MSN
    • Latvia (LV)
    • Lithuania (LT)
      Thiotepa MSN 15 mg milteliai infuzinio tirpalo koncentratui
    • Estonia (EE)
    • Hungary (HU)
      Thiotepa MSN 15 mg por oldatosinfúzióhoz való koncentrátumhoz
    • Bulgaria (BG)
      Thiotepa MSN
    • Czechia (CZ)
      Thiotepa MSN
    • Romania (RO)
      Thiotepa MSN 15 mg pulbere pentru concentrat pentru soluție perfuzabilă
    • Slovakia (SK)
    • Slovenia (SI)
许可日期2025/05/15
最近更新日期2025/05/21
药物ATC编码
    • L01AC01 thiotepa
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
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市场状态Positive
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