欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PT/H/1315/002
药品名称
Tramadol + Paracetamol Aristo
活性成分
paracetamol 650.0 mg
tramadol hydrochloride 75.0 mg
剂型
Film-coated tablet
上市许可持有人
Aristo Pharma Iberia, SL
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Germany (DE)
Tramadol/Paracetamol Aristo 75 mg/650 mg Filmtabletten
Spain (ES)
Italy (IT)
许可日期
2015/07/15
最近更新日期
2024/08/08
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
PubAR
|
588381_588382_20151022_PAR_IRS
Date of last change:2024/09/06
Final Product Information
|
common_inner_combined
Date of last change:2024/09/06
Final Product Information
|
common_outer_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_clean
Date of last change:2024/09/06
Final PL
|
common_pl_tramadol_paracetamol_all_fct_V04_0223
Date of last change:2024/09/06
Final Product Information
|
common_spc_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_tramadol_paracetamol_all_fct_V04_0223
Date of last change:2024/09/06
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase