欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0888/003
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
    • Belgium (BE)
    • Luxembourg (LU)
    • Cyprus (CY)
许可日期2007/02/23
最近更新日期2024/11/01
药物ATC编码
    • N02AX02 tramadol
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • 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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