欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1563/001
药品名称
Moxifloxacina Demo
活性成分
moxifloxacin hydrochloride 454.27 mg
剂型
Film-coated tablet
上市许可持有人
Demo, SA
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Greece (GR)
MOXIFALON T
Cyprus (CY)
MOXIFALON T
许可日期
2016/12/14
最近更新日期
2023/06/01
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 Product Information
|
common_labelling
Date of last change:2024/09/06
Final Product Information
|
common_pil
Date of last change:2024/09/06
Final Product Information
|
common_spc
Date of last change:2024/09/06
PubAR
|
PT_1563_PAR_final
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase