欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1329/001
药品名称
Ciprofloxacina Aurovitas
活性成分
ciprofloxacin hydrochloride 250.0 mg
剂型
Film-coated tablet
上市许可持有人
Aurovitas, Unipessoal, Lda.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Italy (IT)
许可日期
2015/06/17
最近更新日期
2023/11/14
药物ATC编码
J01MA02 ciprofloxacin
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 PL
|
common-pl-annotated
Date of last change:2019/06/28
Final SPC
|
common-spc-annotated
Date of last change:2019/06/28
Final Product Information
|
Clean_Ciprofloxacin Aurovitas film-coated tablets_SPC
Date of last change:2015/06/17
Final Product Information
|
Clean_Ciprofloxacin Aurovitas film-coated tablets_Lab
Date of last change:2015/06/17
Final Product Information
|
Clean_Ciprofloxacin Aurovitas film-coated tablets_PIL
Date of last change:2015/06/17
市场状态
Positive
©2006-2024
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase