欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0538/003
药品名称Tramadol HCl Duiven retard 200 mg, modified release tablets
活性成分
    • Tramadol hydrochloride 200.0 mg
剂型Modified-release tablet
上市许可持有人I.C.C. B.V. Dijkgraaf 30 6921 RL Duiven The Netherlands
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Latvia (LV)
      Mabron SR 200 mg prolonged-release tablets
    • Estonia (EE)
    • Czechia (CZ)
    • Slovakia (SK)
许可日期2005/08/09
最近更新日期2024/10/30
药物ATC编码
    • N02AX02 tramadol
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Generic [Article 10.1.(a)(iii), first paragraph]
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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