欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号CZ/H/0732/001
药品名称Agomelatin Zentiva
活性成分
    • Agomelatine 25.0 mg
剂型Film-coated tablet
上市许可持有人Zentiva k.s. U kabelovny 130 102 37 Praha 10 - Dolní Měcholupy Czech Republic
参考成员国 - 产品名称Czechia (CZ)
AGOMELATIN ZENTIVA
互认成员国 - 产品名称
    • Germany (DE)
      Agomelatin Zentiva 25 mg Filmtabletten
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
    • Portugal (PT)
许可日期2018/05/11
最近更新日期2024/10/31
药物ATC编码
    • N06AX22 agomelatine
申请类型
  • TypeLevel1:Known Active Substance
  • 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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