欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1657/001
药品名称
Moxifloxacina Bloza
活性成分
Moxifloxacin hydrochloride 436.8 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
United Kingdom (Northern Ireland) (XI)
许可日期
2017/08/07
最近更新日期
2024/10/25
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_tracked_Infarmed
Date of last change:2024/09/06
Final PL
|
common_pl_proposed_clean
Date of last change:2024/09/06
Final Labelling
|
common_pl_proposed_track__Infarmed
Date of last change:2024/09/06
Final SPC
|
common_spc_proposed_clean
Date of last change:2024/09/06
Final Labelling
|
common_spc_proposed_track_Infarmed_RevEP
Date of last change:2024/09/06
市场状态
Positive
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