欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IE/H/1029/001
药品名称Paracetamol 500 mg, guaifenesin 100 mg, phenylephrine hydrochloride 6.1 mg, capsule, hard
活性成分
    • paracetamol 500.0 mg
剂型Capsule, hard
上市许可持有人Chefaro Ireland DAC The Sharp Building Hogan Place Dublin 2 Ireland
参考成员国 - 产品名称Ireland (IE)
互认成员国 - 产品名称
    • Lithuania (LT)
    • Estonia (EE)
      COLDREX MAXGRIP
    • Hungary (HU)
    • Bulgaria (BG)
      Coldrex Max Plus Cough
    • Cyprus (CY)
      Solpadeine Cold & Flu
    • Czechia (CZ)
      Coldrex Extra
    • Romania (RO)
      Coldrex MaxGrip Răceală și Tuse capsule
    • Slovakia (SK)
    • Portugal (PT)
    • Slovenia (SI)
      Combocoldrex 500 mg/100 mg/6,1 mg trde kapsule
    • Greece (GR)
    • Croatia (HR)
      Coldrex ComboGrip 500 mg/100 mg/6,1 mg tvrde kapsule
    • Poland (PL)
      Coldrex Complex Grip
    • Latvia (LV)
      Colcaps 500 mg/100 mg/6,1 mg cietās kapsulas
许可日期2021/06/10
最近更新日期2023/02/08
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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase