欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1016/001
药品名称
Cefepima Hospira
活性成分
cefepime dihydrochloride 1000.0 mg
剂型
Powder for solution for infusion/injection
上市许可持有人
Hospira Portugal, Lda.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Belgium (BE)
Latvia (LV)
Slovakia (SK)
Slovenia (SI)
Spain (ES)
Italy (IT)
Poland (PL)
Cefepime Hospira
Hungary (HU)
许可日期
2014/01/23
最近更新日期
2016/11/24
药物ATC编码
J01DE01 cefepime
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 SPC
|
common-spc-19Jan2014
Date of last change:2014/06/05
Final PL
|
common-pl-22Jan2014
Date of last change:2014/06/05
Final Labelling
|
common-label10Jan2014
Date of last change:2014/06/05
市场状态
Positive
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