欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5211/001
药品名称Ezetimibe/Atorvastatine Sandoz 10 mg/10 mg, filmomhulde tabletten
活性成分
    • atorvastatin calcium trihydrate 10.0 mg
    • ezetimibe 10.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Veluwezoom 22, 1327 AH, Almere, Netherlands
参考成员国 - 产品名称Netherlands (NL)
Ezetimibe/Atorvastatine Sandoz 10 mg/10 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Slovenia (SI)
    • Croatia (HR)
      Tulip Combi 10 mg/ 10 mg filmom obložene tablete
    • Belgium (BE)
      Ezetimibe/Atorvastatin Sandoz 10 mg/10 mg filmomhulde tabletten
    • Austria (AT)
      Ezetimib/Atorvastatin 1A Pharma 10 mg/10 mg - Filmtabletten
    • Portugal (PT)
    • Greece (GR)
    • Romania (RO)
许可日期2021/09/26
最近更新日期2024/04/29
药物ATC编码
    • C10BA05 atorvastatin and ezetimibe
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Fixed combination Art 10b 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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