欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/1247/004
药品名称Escita Sandoz 20 mg, filmomhulde tabletten
活性成分
    • escitalopram oxalate 20.0 mg
剂型Film-coated tablet
上市许可持有人New RMS: AT/H/0321/004/DC MAH: Former RMS NL/H/1247/004/DC MAH: Sandoz BV/Almere/NL
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Denmark (DK)
      Escitalopram Sandoz
    • Austria (AT)
      Escitalopram Sandoz 20 mg - Filmtabletten
    • Spain (ES)
    • Portugal (PT)
    • Greece (GR)
    • Poland (PL)
      PRAMATIS
    • Latvia (LV)
      Ciraset 20 mg apvalkotās tabletes
    • Hungary (HU)
      Escitalopram filmtabletta
    • Czechia (CZ)
      Escitalo 20 mg
许可日期2009/01/14
最近更新日期2013/05/21
药物ATC编码
    • N06AB10 escitalopram
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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