欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PT/H/0701/001
药品名称
Moxifloxacina Aurobindo
活性成分
moxifloxacin hydrochloride 400.0 mg
剂型
Film-coated tablet
上市许可持有人
Aurobindo Pharma (Portugal), Unip. Lda.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Germany (DE)
Moxifloxacin Aurobindo 400 mg Filmtabletten
France (FR)
Italy (IT)
许可日期
2012/05/29
最近更新日期
2024/06/13
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
|
Clean_Moxifloxacin Aurobindo_Labelling_10_11_2011
Date of last change:2024/09/06
Final Product Information
|
Clean_Moxifloxacin Aurobindo_PIL_06_04_2012
Date of last change:2024/09/06
Final Product Information
|
Clean_Moxifloxacin Aurobindo_SPC_06_04_2012
Date of last change:2024/09/06
Final PL
|
common_pl
Date of last change:2024/09/06
Final SPC
|
common_spc
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase