欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）

MR编号	NL/H/0423/007
药品名称	Ceftriaxon Sandoz 1 g, powder and solvent for solution for injection/infusion
活性成分	ceftriaxone disodium 1.0 g
剂型	Powder and solvent for solution for injection
上市许可持有人	Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称	Netherlands (NL) Ceftriaxon Sandoz 1 g intraveneus, poeder en oplosmiddel voor oplossing voor injectie/infusie
互认成员国 - 产品名称
许可日期	2010/02/04
最近更新日期	2021/11/11
药物ATC编码	J01DD04 ceftriaxone
申请类型	TypeLevel1：Line Extension TypeLevel2：Additional Strength/Form 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 PL \| common-spc ceftriaxon sandozDate of last change:2021/11/11 Final PL \| common-pl ceftriaxon sandozDate of last change:2021/11/11 Final SPC \| common-spcDate of last change:2021/04/26 Final Product Information \| 1.3.1 spc-label-pl - common-outer - 3,280Date of last change:2017/09/12 Final Product Information \| 1.3.1 spc-label-pl - common-outer - 3,279Date of last change:2017/09/12 Final Product Information \| 1.3.1 spc-label-pl - common-SPC - 2,718Date of last change:2017/09/12 Final Product Information \| 1.3.1 spc-label-pl - common-pl - 8,391Date of last change:2017/09/12 Final Product Information \| 1.3.1 spc-label-pl - common-pl - 8,392Date of last change:2017/09/12 Final Product Information \| 1.3.1 spc-label-pl - common-SPC - 2,719Date of last change:2017/09/12 Final Labelling \| common-labelling NL-H-0423-001--003Date of last change:2015/07/21
市场状态	Positive