欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3089/004
药品名称Escitalopram Magenta 20 mg film-coated tablets
活性成分
    • escitalopram oxalate 20.0 mg
剂型Film-coated tablet
上市许可持有人Magenta Pharma Consulting Ericapark 38 2403 EG Alphen aan den Rijn The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Escitalopram Magenta 20 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
      Escitalopram Magenta 20 mg Filmtabletten
    • France (FR)
    • Ireland (IE)
    • Poland (PL)
      Escitalopram Magenta
    • United Kingdom (GB)
许可日期2015/01/27
最近更新日期2015/11/19
药物ATC编码
    • N06AB10 escitalopram
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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