欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4533/001
药品名称Gaviscon Double Action Liquid
活性成分
    • calcium carbonate 500.0 mg/g
    • sodium bicarbonate 500.0 mg/g
    • sodium chloride 500.0 mg/g
剂型Oral suspension
上市许可持有人Reckitt Benckiser Healthcare (UK) Limited Dansom Lane Hull HU8 7DS United Kingdom
参考成员国 - 产品名称Netherlands (NL)
Gaviscon Duo suspensie, suspensie voor oraal gebruik
互认成员国 - 产品名称
    • Germany (DE)
      Gaviscon Double Action 500 mg/213 mg/325 mg Suspension zum Einnehmen
    • Belgium (BE)
    • Luxembourg (LU)
    • Ireland (IE)
    • Greece (GR)
    • Cyprus (CY)
      GAVISCON DOUBLE ACTION LIQUID
    • Czechia (CZ)
      Gaviscon Double Action Liquid
    • Slovakia (SK)
      Gaviscon Double Action
许可日期2010/05/18
最近更新日期2024/04/23
药物ATC编码
    • A02BX Other drugs for peptic ulcer and gastro-oesophageal reflux disease (GORD)
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
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市场状态Positive
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