欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DK/H/3146/001
药品名称Sitagliptin Mylan
活性成分
    • SITAGLIPTIN 25.0 mg
剂型Film-coated tablet
上市许可持有人Mylan AB Box 230333 10435 Stockholm Sweden
参考成员国 - 产品名称Denmark (DK)
Sitagliptin Mylan
互认成员国 - 产品名称
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
      Sitagliptin Mylan
    • Germany (DE)
      Sitagliptin Mylan 25 mg Filmtabletten
    • Finland (FI)
    • Netherlands (NL)
    • Cyprus (CY)
      Sitagliptin/Mylan 25 mg Film Coated tablets
    • Iceland (IS)
      Sitagliptin Mylan
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
      Sitagliptin Mylan 25 mg Filmtabletten
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
许可日期2021/03/12
最近更新日期2024/01/02
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
附件文件下载
市场状态Positive
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