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

MR编号	NL/H/2977/001
药品名称	Cyclofosfamide Sandoz 500 mg, poeder voor oplossing voor injectie of infusie
活性成分	cyclophosphamide 500.0 mg
剂型	Powder for solution for injection or infusion
上市许可持有人	Sandoz B.V. Veluwezoom 22 1327 AH Almere P.O. box 10332 1301 AH Almere The Netherlands
参考成员国 - 产品名称	Netherlands (NL) Cyclofosfamide Sandoz 500 mg, poeder voor oplossing voor injectie/infusie
互认成员国 - 产品名称	Germany (DE) Cyclophosphamid Hexal 500 mg United Kingdom (Northern Ireland) (XI) France (FR) Hungary (HU) CYCLOPHOSPHAMID SANDOZ 500 mg por oldatos injekcióhoz vagy infúzióhoz
许可日期	2014/07/23
最近更新日期	2024/04/04
药物ATC编码	L01AA01 cyclophosphamide
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 Product Information \| 1.3.1 spc-label-pl - common-spc - TCDate of last change:2021/02/18 Final Product Information \| 1.3.1 spc-label-pl - common-pl - TCDate of last change:2021/02/18 Final SPC \| 1.3.1 spc-label-pl - common-spc - 10,390 - cleanDate of last change:2019/10/12 Final PL \| 1.3.1 spc-label-pl - common-pl - 10,952 - cleanDate of last change:2019/10/12 PAR \| PAR_2977_dc_cyclofosfamide_29 dec 2014Date of last change:2015/02/19 PAR Summary \| PAR_2977_dc_cyclofosfamide_29 dec 2014_summary EngDate of last change:2015/02/19
市场状态	Positive