欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/3895/002
药品名称Atozet 10 mg/20 mg Filmtabletten
活性成分
    • Atorvastatin calcium trihydrate 21.7 mg
    • Ezetimibe 10.0 mg
剂型Film-coated tablet
上市许可持有人Organon Healthcare GmbH Pestalozzistr. 31 80469 München Germany
参考成员国 - 产品名称Germany (DE)
ATOZET 10 mg/20 mg Filmtabletten
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
      Atozet 10mg/20mg comprimés pelliculés
    • Netherlands (NL)
    • Luxembourg (LU)
    • Iceland (IS)
      Atozet 10 mg/20 mg Filmuhúðuð tafla
    • Ireland (IE)
    • Austria (AT)
      Atozet 10 mg/20 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
      LIPTRUZET
    • Sweden (SE)
    • Norway (NO)
      Atozet
    • Cyprus (CY)
      ATOZET FC TABS
    • Czechia (CZ)
      Zoletorv 10 mg/20 mg potahované tablety
    • Malta (MT)
      Atozet 10mg/40mg film-coated tablets
许可日期2014/09/10
最近更新日期2025/09/08
药物ATC编码
    • C10BA05 atorvastatin and ezetimibe
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Fixed combination Art 10b Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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