欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/0701/001
药品名称Sumacta
活性成分
    • sumatriptan succinate 50.0 mg
剂型Film-coated tablet
上市许可持有人Actavis Group PTC ehf Iceland
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Iceland (IS)
    • Latvia (LV)
      Sumatriptan Actavis 50 mg apvalkotās tabletes
    • Lithuania (LT)
      Sumatriptan Actavis 50 mg dengtos tabletes
    • Estonia (EE)
      SUMTRIPTAN ACTAVIS
    • Hungary (HU)
      Sumacta 50-100 mg bevont tabletta
    • Czechia (CZ)
      Sumatriptan Actavis 50 mg
    • Romania (RO)
      Sumacta 50 mg drajeuri
    • Slovenia (SI)
许可日期2007/05/29
最近更新日期2015/06/23
药物ATC编码
    • N02CC01 sumatriptan
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Multiple (Copy) Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
    市场状态Positive
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