欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PT/H/1609/001
药品名称
Moxifloxacina Oara
活性成分
Moxifloxacin hydrochloride 400.0 mg
剂型
Film-coated tablet
上市许可持有人
Bluepharma - Indústria Farmacêutica, S.A.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Poland (PL)
Moxinea
许可日期
2017/01/25
最近更新日期
2022/12/29
药物ATC编码
J01MA14 moxifloxacin
申请类型
TypeLevel1：
Abridged
TypeLevel2：
Initial Application
TypeLevel3：
Generic
TypeLevel4：
Chemical Substance
TypeLevel5：
Prescription Only
附件文件下载
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_11052020_RevEP
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_11052020_RevEP
Date of last change:2024/09/06
市场状态
Positive
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