欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FI/H/1128/002
药品名称
Ceftriaxone Kalceks
活性成分
ceftriaxone sodium salt 2.0 g
剂型
Powder for solution for infusion
上市许可持有人
AS KALCEKS Krustpils iela 71E LV-1057 Riga Latvia
参考成员国 - 产品名称
Finland (FI)
互认成员国 - 产品名称
Latvia (LV)
Lithuania (LT)
-
Hungary (HU)
Germany (DE)
Ceftriaxone Kalceks 2 g Pulver zur Herstellung einer Injektions- bzw. Infusionslösung
Czechia (CZ)
Ceftriaxone Kalceks
Denmark (DK)
Slovenia (SI)
Belgium (BE)
Croatia (HR)
Netherlands (NL)
Poland (PL)
Ceftriaxone Kalceks
Ireland (IE)
Slovakia (SK)
Austria (AT)
France (FR)
Spain (ES)
Norway (NO)
许可日期
2022/11/29
最近更新日期
2024/08/08
药物ATC编码
J01DD04 ceftriaxone
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Other Generic application Art 10.3 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
PubAR
|
Ceftriaxone Kalceks PAR
Date of last change:2024/09/06
Final Labelling
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Final LAB Ceftriaxone Kalceks
Date of last change:2024/09/06
Final PL
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Final PL Ceftriaxone Kalceks
Date of last change:2024/09/06
Final SPC
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Final SPC Ceftriaxone Kalceks
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase