欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5668/002
药品名称Ezetimibe/ Atorvastatine Sandoz 10 mg/20 mg, Film-Coated Tablet
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Sandoz B.V. Veluwezoom 22 1327 AH Almere Flevoland The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Ezetimibe/Atorvastatine Sandoz 10 mg/20mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Hungary (HU)
      Ezetimibe/ Atorvastatine Sandoz 10 mg/20 mg filmtabletta
    • Romania (RO)
    • Slovakia (SK)
    • Germany (DE)
      EzeAtorva 1 A Pharma 10 mg/ 20 mg Filmtabletten
    • Croatia (HR)
    • Belgium (BE)
      Tymyzato 10 mg/20 mg filmomhulde tabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Poland (PL)
      Ezetimibe + Atorvastatin Sandoz
    • Lithuania (LT)
      Ezetimibe/Atorvastatin Sandoz 10 mg/20 mg plėvele dengtos tabletės
许可日期2024/03/13
最近更新日期2024/12/19
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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