欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IS/H/0540/002
药品名称Ezetimibe/Atorvastatin STADA
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STADA Arzneimittel AG Stadastrasse 2-18 61118 Bad Vilbel Germany
参考成员国 - 产品名称Iceland (IS)
Ezetimibe/Atorvastatin STADA
互认成员国 - 产品名称
    • Latvia (LV)
    • Lithuania (LT)
      Atorvastatinas/ezetimibas Kappler 20 mg/10 mg plėvele dengtos tabletės
    • Estonia (EE)
    • Czechia (CZ)
      Ezetimib/Atorvastastin Kappler
    • Slovakia (SK)
    • Germany (DE)
      Ezetimib/Atorvastatin Kappler 10 mg/20 mg Filmtablette
    • Belgium (BE)
    • Luxembourg (LU)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Greece (GR)
许可日期2023/12/19
最近更新日期2024/03/23
药物ATC编码
    • C10BA05 atorvastatin and ezetimibe
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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