欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/4327/002
药品名称Sitagliptin-ratiopharm 50 mg Filmtabletten
活性成分
    • SITAGLIPTIN malate 66.46 mg
剂型Film-coated tablet
上市许可持有人ratiopharm GmbH Graf-Arco-Str. 3 89079 Ulm Germany
参考成员国 - 产品名称Germany (DE)
Sitagliptin-ratiopharm 50 mg Filmtabletten
互认成员国 - 产品名称
    • Denmark (DK)
    • Netherlands (NL)
    • Luxembourg (LU)
      Sitagliptin-ratiopharm, 50 mg, Comprimé pelliculé
    • Iceland (IS)
      Sitagliptin ratiopharm 50 mg Filmuhúðuð tafla
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Sitagliptin ratiopharm 50 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Finland (FI)
    • Poland (PL)
    • Hungary (HU)
      SITAGLIPTIN TEVA 50 mg filmtabletta
    • Slovakia (SK)
      Sitagliptin Teva 50 mg
许可日期2016/07/06
最近更新日期2024/02/02
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
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市场状态Positive
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