欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/5296/002
药品名称Sitagliptine/Metformine HCl Sandoz 50mg/1000 mg, filmomhulde tabletten
活性成分
    • Metformin hydrochloride 1000.0 mg
    • Sitagliptin Hydrochloride monohydrate 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/Metformine HCl Sandoz 50mg/1000 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Estonia (EE)
    • Hungary (HU)
    • Czechia (CZ)
      Sitagliptin/Metformin Sandoz GmbH
    • Slovakia (SK)
    • Austria (AT)
    • Malta (MT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Greece (GR)
    • Finland (FI)
    • Latvia (LV)
    • Lithuania (LT)
      Metformin hydrochloride/Sitagliptin Sandoz 1000 mg/50 mg plėvele dengtos tabletės
许可日期2022/02/10
最近更新日期2024/10/31
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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