欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/1621/001
药品名称Tamsulijn 0.4 mg
活性成分
    • tamsulosin hydrochloride 0.4 mg
剂型Prolonged-release capsule, hard
上市许可持有人Synthon B.V. Microweg 22 6545 CM Nijmegen, Gelderland Netherlands Former procedure FI/H/0506/001/
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Cyprus (CY)
      Tamsulijn 0.4 mg Modified release capsule, hard
    • Germany (DE)
    • Iceland (IS)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Tamsulijn retard 0,4 mg Kapseln
    • France (FR)
    • Greece (GR)
    • Estonia (EE)
      FLOSIN 0,4MG
    • Lithuania (LT)
      Flosin 0,4 mg modifikuoto atpalaidavimo kietos kapsulės
    • Poland (PL)
      Flosin 0,4 mg
    • Hungary (HU)
许可日期2009/06/26
最近更新日期2024/07/05
药物ATC编码
    • G04CA02 tamsulosin
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
    市场状态Positive
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