欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3001/004
药品名称Memantine hydrochloride 20 mg
活性成分
    • Memantine hydrochloride 20.0 mg
剂型Film-coated tablet
上市许可持有人Medochemie Ltd 1-10 Constantinoupoleos Street, Limassol 3011 Cyprus
参考成员国 - 产品名称Netherlands (NL)
Mantomed 20 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Latvia (LV)
    • Slovenia (SI)
    • Greece (GR)
      AVANTEN
    • Lithuania (LT)
      MANTOMED 20 mg plėvele dengtos tabletės
    • Estonia (EE)
      MANTOMED
    • Cyprus (CY)
    • Czechia (CZ)
      Avanten 20 mg potahované tablety
    • Romania (RO)
      MANTOMED 20 mg comprimate filmate
    • Slovakia (SK)
    • Spain (ES)
    • Croatia (HR)
许可日期2014/09/11
最近更新日期2024/10/28
药物ATC编码
    • N06DX01 memantine
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Additional Strength/Form
  • 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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