欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号HU/H/0851/002
药品名称Dimethyl Fumarate Gedeon Richter 240 mg, gastro-resistant hard capsule
活性成分
    • dimethyl fumarate 240.0 mg
剂型Gastro-resistant capsule, hard
上市许可持有人Gedeon Richter Polska Sp. z o.o. Ul. Ks. Jozefa Poniatowskiego 5 Grodzisk Mazowiecki Mazowieckie 05-825 Poland Telephone +48 22 755 96 62 E-mail gedeonPLMRP@grodzisk.rgnet.org
参考成员国 - 产品名称Hungary (HU)
互认成员国 - 产品名称
    • Poland (PL)
      Dimethyl Fumarate Gedeon Richter
    • Latvia (LV)
    • Lithuania (LT)
      TYXENOS 240 mg skrandyje neirios kietosios kapsulės
    • Estonia (EE)
    • Bulgaria (BG)
      Demiron
    • Czechia (CZ)
      DEMIRON
    • Romania (RO)
      DEMIRON 240 mg capsule gastrorezistente
    • Slovakia (SK)
许可日期2024/01/31
最近更新日期2025/02/10
药物ATC编码
    • L04AX07 dimethyl fumarate
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
附件文件下载
    市场状态Positive
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