欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/1550/001
药品名称Jimandin
活性成分
    • SITAGLIPTIN 25.0 mg
剂型Film-coated tablet
上市许可持有人Medochemie Ltd. Cyprus
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Lithuania (LT)
      JIMANDIN 25 mg plėvele dengtos tabletės
    • Estonia (EE)
      JIMANDIN
    • Cyprus (CY)
    • Romania (RO)
      JIMANDIN 25 mg comprimate filmate
    • Malta (MT)
      Jimandin 25 mg film-coated tablets
    • Croatia (HR)
      Jimandin 25 mg filmom obložene tablete
许可日期2017/06/21
最近更新日期2021/12/02
药物ATC编码
    • A10BH01 sitagliptin
申请类型
  • TypeLevel1:Known Active Substance
  • 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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