欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PL/H/0592/002
药品名称
Ibu[profen Teva MAX
活性成分
ibuprofen lysin salt 684.0 mg
剂型
Film-coated tablet
上市许可持有人
Teva Pharmaceuticals Polska Sp. z o.o.
参考成员国 - 产品名称
Poland (PL)
互认成员国 - 产品名称
许可日期
2012/03/08
最近更新日期
2021/02/03
药物ATC编码
M01AE01 ibuprofen
申请类型
TypeLevel1：
[not specified]
TypeLevel2：
[not specified]
TypeLevel3：
[not specified]
TypeLevel4：
[not specified]
TypeLevel5：
[not specified]
附件文件下载
Final Labelling
|
DE_H_2589_90_Ibuprofen lysine 342_684 mg film_coated tablets_ImP_clean_20150901_renewal
Date of last change:2024/09/06
Final Labelling
|
DE_H_2589_90_Ibuprofen lysine 342_684 mg film_coated tablets_outer_clean_20150901_renewal
Date of last change:2024/09/06
Final SPC
|
DE_H_2589_90_Ibuprofen lysine 342_684 mg film_coated tablets_SmPC_clean_20150901_renewal
Date of last change:2024/09/06
Final PL
|
DE_H_2589_Ibuprofen lysine 342 mg film_coated tablets_PIL_clean_20150901_renewal
Date of last change:2024/09/06
Final PL
|
DE_H_2590_Ibuprofen lysine 684 mg film_coated tablets_PIL_clean_20150901_renewal
Date of last change:2024/09/06
Final Labelling
|
DE_H_2605_1_2_Irfen L_DCP_olab_clean_20150901_renewal
Date of last change:2024/09/06
Final PL
|
DE_H_2605_1_2_Irfen L_DCP_PIL_clean_20150901_renewal
Date of last change:2024/09/06
Final SPC
|
DE_H_2605_1_2_Irfen L_DCP_SmPC_clean_20150901_renewal
Date of last change:2024/09/06
Final Product Information
|
final_common_2605_017Outer Packaging
Date of last change:2024/09/06
Final Product Information
|
final_common_2605_017PL
Date of last change:2024/09/06
Final Product Information
|
final_common_2605_017SPC
Date of last change:2024/09/06
PubAR
|
PAREN_DE2605_Irfen
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase