欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/2156/001
药品名称Esomeprazol SUN 40 mg powder for solution for injection / infusion
活性成分
    • esomeprazole sodium salt 40.0 mg
剂型Powder for solution for infusion/injection
上市许可持有人SUN Pharmaceutical Industries Europe BV Polarisavenue 87 2132 JH hoofddorp
参考成员国 - 产品名称Netherlands (NL)
Esomeprazol SUN 40 mg poeder voor oploosing voor injectie en intraveneuze infusie
互认成员国 - 产品名称
    • Romania (RO)
      Esomeprazol SUN 40 mg pulbere pentru soluţie injectabilă și perfuzabilă
    • Germany (DE)
      Esomeprazol Sun 40 mg Pulver zur Herstellung einer Injektions-/Infusionslösung
    • Denmark (DK)
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
    • Italy (IT)
    • Sweden (SE)
      Esomeprazol Sun
    • Poland (PL)
      Esomeprazol SUN
许可日期2011/10/19
最近更新日期2023/12/07
药物ATC编码
    • A02BC05 esomeprazole
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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