欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3783/002
药品名称Ivabradine Mylan 7.5 mg film-coated tablets
活性成分
    • ivabradine oxalate 7.5 mg
剂型Film-coated tablet
上市许可持有人Mylan B.V. Dieselweg 25 3752 LB Bunschoten the Netherlands
参考成员国 - 产品名称Netherlands (NL)
Ivabradine Mylan 7,5 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Germany (DE)
      Ivabradine 7,5 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Poland (PL)
      Ivabradine Mylan
    • Latvia (LV)
      Ivabradine Mylan 7,5 mg apvalkotās tabletes
    • Lithuania (LT)
      Ivabradine Mylan 7,5 mg plėvele dengtos tabletės
    • Estonia (EE)
      IVABRADINE MYLAN
    • Bulgaria (BG)
      Ivabradin AET
    • Slovakia (SK)
      Ivabradine Mylan 7,5 mg filmom obalené tablety
    • United Kingdom (Northern Ireland) (XI)
许可日期2016/10/20
最近更新日期2024/04/10
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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