欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号SE/H/2628/006
药品名称Dibaglep
活性成分
    • Dapagliflozin 10.0 mg
    • Sitagliptin 100.0 mg
剂型Film-coated tablet
上市许可持有人Viatris Limited Ireland
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Romania (RO)
      Dibaglep 100 mg/ 10 mg comprimate filmate
    • Malta (MT)
    • Croatia (HR)
    • Denmark (DK)
      Dibaglep
    • Belgium (BE)
    • Luxembourg (LU)
    • Portugal (PT)
      Dibaglep
    • Italy (IT)
    • Greece (EL)
    • Cyprus (CY)
      Dibaglep Film-coated tablet, 100 mg/10 mg
    • Czech Republic (CZ)
      Dibaglep
许可日期2025/11/19
最近更新日期2025/12/19
药物ATC编码
    • A10BD29 sitagliptin and dapagliflozin
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Additional Strength/Form
  • TypeLevel3：Fixed Combination
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
附件文件下载
    市场状态Positive
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