欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）

MR编号	NL/H/0483/003
药品名称	MP-Tramadol HCl retard 200
活性成分	tramadol hydrochloride 200.0 mg
剂型	Modified-release tablet
上市许可持有人	Sandoz B.V Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称	Netherlands (NL)
互认成员国 - 产品名称	United Kingdom (Northern Ireland) (XI)
许可日期	2004/08/26
最近更新日期	2022/05/25
药物ATC编码	N02AX02 tramadol
申请类型	TypeLevel1：Abridged TypeLevel2：Additional Strength/Form TypeLevel3：Generic Article 4.8(a)(iii), first paragraph TypeLevel4：Chemical Substance TypeLevel5：Prescription Only
附件文件下载	Final SPC \| common_spc_2Date of last change:2021/07/22 Final PL \| common_pl_100mg_2Date of last change:2021/07/22 Final PL \| common-pl-150mg_2Date of last change:2021/07/22 Final PL \| common-pl-200mg_2Date of last change:2021/07/22 Final Labelling \| 1.3.1 spc-label-pl - common-outer - 4,728CLEANDate of last change:2018/11/26 Final Product Information \| common-outerDate of last change:2016/11/11 Final Product Information \| common-pl-100mgDate of last change:2016/11/11 Final Product Information \| common-pl-150mgDate of last change:2016/11/11 Final Product Information \| common-pl-200mgDate of last change:2016/11/11 Final Product Information \| common-spcDate of last change:2016/11/11
市场状态	Positive