欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0238/003
药品名称
Ciprofloxacin Mylan
活性成分
ciprofloxacin hydrochloride 500.0 mg
剂型
Film-coated tablet
上市许可持有人
Viatris Limited, Ireland
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Belgium (BE)
Ciprofloxacine Viatris 500 mg filmomhulde tabletten
Netherlands (NL)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
Portugal (PT)
Italy (IT)
许可日期
2001/03/18
最近更新日期
2024/03/13
药物ATC编码
J01MA02 ciprofloxacin
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Generic Article 4.8(a)(iii), first paragraph
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final SPC
|
SE_H_0238_003_Final SPC
Date of last change:2023/08/23
Final PL
|
SE_H_0238_003_Final PL
Date of last change:2023/08/23
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase