欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4976/002
药品名称Sitagliptine/Metformine HCl 50/1000 mg
活性成分
    • metformin hydrochloride 1000.0 mg
    • Sitagliptin Hydrochloride 50.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V., Veluwezoom 22, 1327 AH, Almere, Nederland
参考成员国 - 产品名称Netherlands (NL)
Sitagliptine/Metformine HCl Sandoz 50/1000 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Norway (NO)
      Sitagliptin/Metformin Sandoz
    • Finland (FI)
    • Hungary (HU)
      Sitagliptin/Metformin Sandoz 50 mg/1000 mg filmtabletta
    • Denmark (DK)
    • Czechia (CZ)
      Sitagliptin/Metformin Sandoz
    • Belgium (BE)
      Sitagliptin/Metformin Sandoz 50 mg/1000 mg filmomhulde tabletten
    • Iceland (IS)
    • Austria (AT)
      Sitagliptin/Metformin Sandoz 50 mg/1000 mg – Filmtabletten
    • France (FR)
    • Estonia (EE)
    • Spain (ES)
    • Portugal (PT)
    • Sweden (SE)
      Sitagliptin/Metformin Sandoz
许可日期2021/01/08
最近更新日期2024/05/13
药物ATC编码
    • A10BD07 metformin and 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
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市场状态Positive
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