欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3622/003
药品名称Ivabradine Synthon 7.5mg film-coated tablets
活性成分
    • ivabradine hydrochloride 7.5 mg
剂型Film-coated tablet
上市许可持有人Synthon BV, Microweg 22, 6545 CM Nijrnegen, The Netherlands
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • France (FR)
    • Greece (GR)
      IVABRADINE/SYNTHON
    • Poland (PL)
      Iwabradyna Synthon
许可日期2016/12/15
最近更新日期2023/04/12
药物ATC编码
    • C01EB17 ivabradine
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
附件文件下载
市场状态Positive
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