欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SK/H/0302/001
药品名称Linagliptin Viatris
活性成分
    • linagliptin 5.0 mg
剂型Film-coated tablet
上市许可持有人Viatris Limited Damastown Road, Damastown Industrial Park Dublin 15 D15 XD71, Ireland
参考成员国 - 产品名称Slovakia (SK)
互认成员国 - 产品名称
    • Denmark (DK)
      Linagliptin Viatris
    • Netherlands (NL)
    • Ireland (IE)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Bulgaria (BG)
      Linagliptin Viatris
    • Czechia (CZ)
      Linagliptin Viatris
许可日期2023/12/29
最近更新日期2025/01/29
药物ATC编码
    • A10BH05 linagliptin
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
附件文件下载
市场状态Positive
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