欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号CZ/H/1010/002
药品名称Sitagliptin Zentiva
活性成分
    • Sitagliptin Hydrochloride monohydrate 50.0 mg
剂型Film-coated tablet
上市许可持有人Viatris Limited, Damastown Industrial Park, Mulhuddart, Dublin 15, Dublin, Ireland
参考成员国 - 产品名称Czech Republic (CZ)
Sitagliptin Zentiva
互认成员国 - 产品名称
    • Greece (EL)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • United Kingdom (Northern Ireland) (XI)
    • Germany (DE)
      Sitagliptin Zentiva
    • Denmark (DK)
    • Iceland (IS)
      Sitagliptin Zentiva
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
许可日期2021/11/03
最近更新日期2025/12/08
药物ATC编码
    • A10BH01 sitagliptin
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Generic
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
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市场状态Positive
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