欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号AT/H/1183/002
药品名称Sitagliptin/Metformin 50 mg/1000 mg filmcoated tablets
活性成分
    • metformin hydrochloride 1000.0 mg
    • SITAGLIPTIN 50.0 mg
剂型Film-coated tablet
上市许可持有人Reddy Holding GmbH Kobelweg 95 86156 Augsburg Germany
参考成员国 - 产品名称Austria (AT)
Sitagliptin/Metformin Reddy 50 mg/1000 mg Filmtabletten
互认成员国 - 产品名称
    • Poland (PL)
      Sytagliptyna + Metforminy chlorowodorek Reddy
    • Czechia (CZ)
      Sitagliptinum/Metformini Reddy
    • Romania (RO)
      SitagliptinăMetformin Dr. Reddy’s 50/1000 mg comprimate filmate
    • Germany (DE)
      Sitagliptin/Metformin beta 50 mg / 1000 mg Filmtabletten
    • Slovakia (SK)
    • Denmark (DK)
    • Netherlands (NL)
      Sitagliptine/Metformine Reddy 50 mg/1000 mg filmomhulde tabletten
    • France (FR)
    • Spain (ES)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
许可日期2022/05/11
最近更新日期2024/06/06
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
附件文件下载
市场状态Positive
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