欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/6004/003
药品名称Treprostinil Tillomed 5 mg/ml Infusionslösung
活性成分
    • Treprostinil 5.0 mg/ml
剂型Solution for infusion
上市许可持有人TILLOMED PHARMA GmbH Mittelstraße 5/5a 12529 Schönefeld Germany
参考成员国 - 产品名称Germany (DE)
Treprostinil Tillomed 5 mg/ml Infusionslösung
互认成员国 - 产品名称
    • Austria (AT)
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
      Treprostinil Tillomed
    • Lithuania (LT)
      Treprostinil Tillomed 5 mg/ml infuzinis tirpalas
    • Hungary (HU)
      TREPROSTINIL TILLOMED 5 mg/ml oldatos infúzió
    • Czechia (CZ)
      Treprostinil Tillomed 5 mg / ml infuzního roztoku
    • Slovakia (SK)
    • Slovenia (SI)
    • Croatia (HR)
      Treprostinil Tillomed 5 mg/ml otopina za infuziju
许可日期2020/06/10
最近更新日期2025/04/25
药物ATC编码
    • B01AC21 treprostinil
申请类型
  • TypeLevel1：Abridged
  • 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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