欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号CZ/H/0984/001
药品名称Tramadol/Paracetamol Medreg
活性成分
    • paracetamol 325.0 mg
    • tramadol hydrochloride 37.5 mg
剂型Film-coated tablet
上市许可持有人Medreg s.r.o. Krčmářovská 223/33 Prague 196 00 Czech Republic
参考成员国 - 产品名称Czechia (CZ)
Tramadol/Paracetamol Medreg
互认成员国 - 产品名称
    • Poland (PL)
      Tramadol + Paracetamol Medreg
    • Romania (RO)
      Tramadol/Paracetamol Medreg 37,5 mg/325 mg comprimate filmate
    • Slovakia (SK)
      Tramadol/Paracetamol Medreg
许可日期2021/01/19
最近更新日期2024/08/19
药物ATC编码
    • N02AJ13 tramadol and paracetamol
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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