欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
DE/H/5687/002
药品名称
IbuARISTO 400 mg
活性成分
ibuprofen 400.0 mg
剂型
Film-coated tablet
上市许可持有人
Aristo Pharma GmbH Wallenroder Str. 8-10 D-13435 Berlin Germany
参考成员国 - 产品名称
Germany (DE)
IbuARISTO 400 mg Filmtabletten
互认成员国 - 产品名称
Denmark (DK)
Portugal (PT)
Sweden (SE)
许可日期
2019/11/18
最近更新日期
2024/11/26
药物ATC编码
M01AE01 ibuprofen
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
附件文件下载
Final SPC
|
common_final_spc_DE5687_002__V010
Date of last change:2024/09/12
Final PL
|
common_final_pl_DE5687_002__V010
Date of last change:2024/09/12
PubAR
|
2202419_2202404_06_PAREN_DE 5687_Ibuprofen
Date of last change:2024/09/06
Final Product Information
|
common_final_labip_5687_001__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_labip_5687_002__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_labip_5687_003__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_labip_5687_004__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_labop_5687_001__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_labop_5687_002__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_labop_5687_003__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_labop_5687_004__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_pl_5687_001__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_pl_5687_002__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_pl_5687_003__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_pl_5687_004__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_spc_5687_001__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_spc_5687_002__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_spc_5687_003__V002
Date of last change:2024/09/06
Final Product Information
|
common_final_spc_5687_004__V002
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase