欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号IE/H/0760/001
药品名称Benylin Day & Night Tablets 500mg, pseudoephedrine hydrochloride 60mg 500mg, diphenhydramine hydrochloride 25mg
活性成分
    • Paracetamol hydrochloride 500.0 mg
剂型Tablet
上市许可持有人Johnson & Johnson Ireland Limited Airton Road Tallaght Dublin 24 Ireland
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Greece (GR)
    • Bulgaria (BG)
      Olygrip Day and Night
    • Cyprus (CY)
      Hexaflu Day & Night, 500/60mg & 500/25mg Tablets
    • Romania (RO)
      Olygrip Day and Night comprimate
许可日期2020/05/28
最近更新日期2025/03/18
药物ATC编码
    • N02BE51 paracetamol, combinations excl. psycholeptics
申请类型
  • TypeLevel1：Known Active Substance
  • TypeLevel2：Initial Application
  • TypeLevel3：Bibliographic Art 10 a 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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