欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4425/001
药品名称Saxagliptin HCl Sandoz 2.5 mg, film-coated tablets
活性成分
    • Saxagliptin Hydrochloride Dihydrate 2.79 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Saxagliptine HCl Sandoz 2,5 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
许可日期2019/05/03
最近更新日期2024/10/18
药物ATC编码
    • A10BH03 saxagliptin
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
附件文件下载
市场状态Positive
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