欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号ES/H/0818/001
药品名称Remidol 650 mg/20 mg/4 mg powder for oral solution
活性成分
    • chlorphenamine maleate 4.0 mg
    • dextromethorphan hydrobromide 20.0 mg
    • paracetamol 650.0 mg
剂型Powder for oral solution
上市许可持有人Farmasierra Laboratorios S.L. Carretera De Irun Km. 26,200 San Sebastian De Los Reyes, 28700 Madrid (Spain)
参考成员国 - 产品名称Spain (ES)
互认成员国 - 产品名称
    • Italy (IT)
许可日期2021/09/03
最近更新日期2023/11/14
药物ATC编码
    • N02BE51 paracetamol, combinations excl. psycholeptics
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:Non Prescription (including OTC)
附件文件下载
市场状态Positive
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