欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1016/002
药品名称
Cefepima Hospira
活性成分
Cefepime dihydrochloride 2000.0 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)
Italy (IT)
Poland (PL)
Cefepime Hospira
Hungary (HU)
许可日期
2014/01/23
最近更新日期
2024/12/12
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 Labelling
|
common_label10Jan2014
Date of last change:2024/09/06
Final PL
|
common_pl_22Jan2014
Date of last change:2024/09/06
Final SPC
|
common_spc_19Jan2014
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase