欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DK/H/1193/001
药品名称Medi-MIBI
活性成分
    • Tetrakis(1-isocyan-2-methoxy-2-methylpropan)copper(1)-tetrafluoroborat 0.5 mg
剂型Radiopharmaceutical kit
上市许可持有人Radiopharmacy Laboratory Ltd. 2040 Budaörs, Gyár st. 2. Hungary
参考成员国 - 产品名称Denmark (DK)
互认成员国 - 产品名称
    • Luxembourg (LU)
    • Cyprus (CY)
      Medi-MIBI Kit for radiopharmaceutical preparation, 0.5 mg
    • Netherlands (NL)
      Medi-MIBI 0,5 mg, Kit voor radiofarmaceutisch preparaat
    • Malta (MT)
      Medi-Mibi Kit for Radiopharmaceutical Preparation 0.5mg
    • Portugal (PT)
    • Slovenia (SI)
    • Estonia (EE)
    • Slovakia (SK)
    • Greece (GR)
    • Finland (FI)
    • Austria (AT)
      Medi-MIBI 500 Mikrogramm Kit für ein radioaktives Arzneimittel
    • Spain (ES)
    • Italy (IT)
    • Lithuania (LT)
    • Latvia (LV)
    • Norway (NO)
    • Belgium (BE)
      Medimibi 0,5 mg kit voor radiofarmaceutisch preparaat
    • Poland (PL)
      Medi-MIBI
    • France (FR)
    • Sweden (SE)
许可日期2008/01/21
最近更新日期2024/04/24
药物ATC编码
    • V09GA01 technetium (99mTc) sestamibi
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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