欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/5473/003
药品名称Broxil 125 mg/5 ml poeder voor orale suspensie
活性成分
    • pheneticillin potassium 25.0 mg/ml
剂型Powder for oral suspension
上市许可持有人ACE Pharmaceuticals BV Schepenveld 41 3891 ZK Zeewolde Nederland
参考成员国 - 产品名称Netherlands (NL)
Broxil 125 mg/5 ml poeder voor orale suspensie RVG 02672
互认成员国 - 产品名称
    • Belgium (BE)
      Broxil 125 mg / 5 ml poeder voor orale suspensie
许可日期2021/07/30
最近更新日期2023/10/30
药物ATC编码
    • J01CE05 pheneticillin
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Full Dossier Art 8.3(i) Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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