欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5122/002
药品名称Ezetimibe/Atorvastatine Teva 10 mg/20 mg, filmomhulde tabletten
活性成分
    • atorvastatin calcium trihydrate 20.0 mg
    • ezetimibe 10.0 mg
剂型Film-coated tablet
上市许可持有人Teva B.V. Swensweg 5, 2031GA Haarlem, The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Ezetimibe/Atorvastatine Teva 10 mg/20 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Belgium (BE)
    • Bulgaria (BG)
      Avanor Plus
    • Luxembourg (LU)
    • Germany (DE)
      Ezesta 10 mg/20 mg Filmtabletten
    • Slovakia (SK)
    • Austria (AT)
      Ezetimib/Atorvastatin ratiopharm 10 mg/20 mg Filmtabletten
    • Portugal (PT)
    • Croatia (HR)
      Co-Atorvox 10 mg/20 mg filmom obložene tablete
许可日期2021/05/25
最近更新日期2024/04/29
药物ATC编码
    • C10BA05 atorvastatin and ezetimibe
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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