欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PT/H/2372/001
药品名称Paracetamol/Guaifenesin/Phenylephrine 500mg/200mg/10mg Powder for oral solution
活性成分
    • guaifenesin 200.0 mg
    • paracetamol 500.0 mg
    • PHENYLEPHRINE HYDROCHLORIDE 10.0 mg
剂型Powder for oral solution
上市许可持有人17/6/19
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • Spain (ES)
    • Latvia (LV)
      Hotex 500 mg/200 mg/10 mg pulveris iekšķīgi lietojama šķīduma pagatavošanai
    • Lithuania (LT)
    • Estonia (EE)
    • Hungary (HU)
      COLDREX PLUS köhögés elleni por belsőleges oldathoz
    • Slovenia (SI)
      Paracetamol/gvaifenezin/fenilefrin Adriatic BST 500 mg/200 mg/10 mg prašek za peroralno raztopino
    • Croatia (HR)
      Coldrex ComboGrip 500 mg/200 mg/10 mg prašak za oralnu otopinu
许可日期2017/09/23
最近更新日期2024/01/22
药物ATC编码
    • N02BE51 paracetamol, combinations excl. psycholeptics
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
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市场状态Positive
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