欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/7734/002
药品名称Cadelta
活性成分
    • Apixaban 5.0 mg
剂型Film-coated tablet
上市许可持有人Egis Gyogyszergyar Zrt. Kereszturi Ut 30-38 1106 Budapest X Hungary
参考成员国 - 产品名称Germany (DE)
CADELTA 5 mg Filmtabletten
互认成员国 - 产品名称
    • Hungary (HU)
      Cadelta 5 mg filmtabletta
    • Bulgaria (BG)
      CADELTA
    • Czechia (CZ)
      Cadelta
    • Romania (RO)
      CADELTA 5 mg comprimate filmate
    • Slovakia (SK)
    • Poland (PL)
      Cadelta
    • Latvia (LV)
    • Lithuania (LT)
许可日期2024/11/06
最近更新日期2024/11/14
药物ATC编码
    • B01AF02 apixaban
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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