欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/4937/001
药品名称Sitagliptine CF 25 mg, filmomhulde tabletten
活性成分
    • Sitagliptin hydrochloride 25.0 mg
剂型Film-coated tablet
上市许可持有人Centrafarm B.V. Van de Reijstraat 31E 4814 NE Breda The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Sitagliptine CF 25 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Luxembourg (LU)
    • Iceland (IS)
    • Austria (AT)
      Sitagliptin STADA 25 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Greece (GR)
    • Sweden (SE)
    • Finland (FI)
    • Germany (DE)
      Sitagliptin STADA 25 mg Filmtabletten
    • Denmark (DK)
许可日期2021/09/08
最近更新日期2024/11/19
药物ATC编码
    • A10BH01 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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