欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/2514/001
药品名称Escitalopram 20 mg/ml druppels voor oraal gebruik, oplossing
活性成分
    • Escitalopram oxalate 20.0 mg/ml
剂型Oral drops, solution
上市许可持有人Chanelle Medical Unlimited Company Dublin Road H62 FH90 Loughrea, Co. Galway Ireland
参考成员国 - 产品名称Netherlands (NL)
Escitalopram 20 mg/ml druppels voor oraal gebruik, oplossing
互认成员国 - 产品名称
    • Germany (DE)
      Escitalopram 20mg/ml Tropfen zum Einnehmen, Lösung
    • Italy (IT)
    • Poland (PL)
      Betesda
许可日期2012/11/12
最近更新日期2024/11/22
药物ATC编码
    • N06AB10 escitalopram
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
附件文件下载
市场状态Positive
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