欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号EE/H/0266/001
药品名称Diclopram
活性成分
    • diclofenac sodium 75.0 mg
    • omeprazole 20.0 mg
剂型Modified-release capsule, hard
上市许可持有人Bausch Health Ireland Limited 3013 Lake Drive Citywest Business Campus Dublin 24 Ireland
参考成员国 - 产品名称Estonia (EE)
互认成员国 - 产品名称
    • Greece (GR)
      DICLODUO COMBI
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
      DIOMPRAZ 75 mg/20 mg modifikuoto atpalaidavimo kietosios kapsulės
    • Hungary (HU)
      DIOM 75 mg/20 mg módosított hatóanyagleadású kemény kapszula
    • Bulgaria (BG)
    • Cyprus (CY)
      DICLODUO COMBI MR HARD CAPS
    • Slovakia (SK)
      DIOMPRAZ 75 mg/20 mg tvrdé kapsuly s riadeným uvoľňovaním
    • Malta (MT)
      DICLODUO COMBI 75 mg / 20 mg, modified release hard
许可日期2014/09/09
最近更新日期2023/04/10
药物ATC编码
    • M01AB55 diclofenac, combinations
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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