欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0992/003
药品名称
Ceftriaxona Hospira
活性成分
ceftriaxone sodium salt 1.0 g
剂型
Powder for solution for injection
上市许可持有人
Hospira UK Limited
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Bulgaria (BG)
Slovakia (SK)
Malta (MT)
Poland (PL)
Romania (RO)
Lithuania (LT)
Latvia (LV)
Estonia (EE)
Slovenia (SI)
Belgium (BE)
Ceftriaxone Hospira 1 g Poeder voor oplossing voor injectie
United Kingdom (Northern Ireland) (XI)
Ceftriaxona Hospira
Ireland (IE)
Italy (IT)
Cyprus (CY)
CEFTRIAXONE HOSPIRA PWD FOR SOL FOR INJ
许可日期
2014/01/22
最近更新日期
2024/05/28
药物ATC编码
J01DD04 ceftriaxone
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
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市场状态
Positive
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