欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/4930/002
药品名称Sitagliptine Sandoz 50 mg, filmomhulde tabletten
活性成分
    • SITAGLIPTIN 50.0 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)
Sitagliptine Sandoz 50 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Belgium (BE)
      Sitagliptin Sandoz
    • Iceland (IS)
      Sitagliptin Sandoz
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Sitagliptin Sandoz 50 mg – Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Estonia (EE)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Denmark (DK)
    • Hungary (HU)
许可日期2021/02/17
最近更新日期2023/11/09
药物ATC编码
    • A10BH01 sitagliptin
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Additional Strength/Form
  • 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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase