欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0776/001
药品名称
Tramadol + Paracetamol Bristol
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
Bristol Laboratories Ltd.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Poland (PL)
Tramadol hydrochloride + Paracetamol Bristol Laboratories
许可日期
2013/05/30
最近更新日期
2023/01/10
药物ATC编码
N02AX52 tramadol, combinations
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Product Information
|
common_impack_clean
Date of last change:2024/09/06
Final Product Information
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common_outer_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_clean
Date of last change:2024/09/06
Final Product Information
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common_spc_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase