欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/6676/001
药品名称Sitagliptin/Metformin AbZ 50 mg/850 mg Filmtabletten
活性成分
    • Metformin hydrochloride 850.0 mg
    • Sitagliptin 50.0 mg
剂型Film-coated tablet
上市许可持有人AbZ-Pharma GmbH Graf-Arco-Str. 3 89079 Ulm Germany
参考成员国 - 产品名称Germany (DE)
Metformin/Sitagliptin AbZ 850 mg/50 mg Filmtabletten
互认成员国 - 产品名称
    • Slovakia (SK)
    • Netherlands (NL)
    • Ireland (IE)
    • Austria (AT)
    • Portugal (PT)
    • Italy (IT)
    • Finland (FI)
    • Latvia (LV)
    • Lithuania (LT)
      -
    • Estonia (EE)
      Sitagliptin/Metformin hydrochloride Teva
    • Hungary (HU)
    • Czechia (CZ)
      METFORMIN/SITAGLIPTIN TEVA
许可日期2021/12/15
最近更新日期2025/02/11
药物ATC编码
    • A10BD07 metformin and sitagliptin
申请类型
  • TypeLevel1：Abridged
  • 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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