欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号PT/H/0919/002
药品名称Tramadol + Paracetamol PTR
活性成分
    • tramadol hydrochloride 75.0 mg
    • paracetamol 650.0 mg
剂型Tablet
上市许可持有人PTR Pharma Consulting, Lda
参考成员国 - 产品名称Portugal (PT)
Tramadol + Paracetamol Litexil
互认成员国 - 产品名称
    • Hungary (HU)
    • Poland (PL)
      Delparan Max
    • Romania (RO)
      Tramadol/Paracetamol Sandoz 75 mg/650 mg comprimate
    • Slovenia (SI)
    • Slovakia (SK)
    • Denmark (DK)
    • Luxembourg (LU)
    • Czechia (CZ)
      Tramadol/paracetamol Sandoz 75 mg/620 mg
    • Sweden (SE)
    • Norway (NO)
    • Croatia (HR)
      Tramadolor DUO 75 mg/650 mg tablete
许可日期2013/03/27
最近更新日期2024/01/02
药物ATC编码
    • N02AJ13 tramadol and paracetamol
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
市场状态Positive
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