欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PT/H/1734/001
药品名称
Moxifloxacina Bluesar
活性成分
moxifloxacin hydrochloride 454.27 mg
剂型
Film-coated tablet
上市许可持有人
Bluepharma
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Poland (PL)
许可日期
2017/01/25
最近更新日期
2022/08/02
药物ATC编码
J01MA14 moxifloxacin
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 Labelling
|
common_interpack_proposed_tracked
Date of last change:2024/09/06
Final Product Information
|
common_outer_moxifloxacin_trackchanges
Date of last change:2024/09/06
Final Product Information
|
common_pl_moxifloxacin_trackchanges
Date of last change:2024/09/06
Final PL
|
common_pl_proposed_track
Date of last change:2024/09/06
Final Product Information
|
common_spc_moxifloxacin_trackchanges
Date of last change:2024/09/06
Final SPC
|
common_spc_proposed_track_RevEP
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase