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

MR编号	NL/H/0301/001
药品名称	Ciprofloxacine Sandoz 250 mg, filmomhulde tabletten
活性成分	Ciprofloxacin as ciprofloxacin hydrochloride 250.0 mg
剂型	Film-coated tablet
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)
互认成员国 - 产品名称	Germany (DE) Denmark (DK) Belgium (BE) Austria (AT) Ciprofloxacin 1A Pharma 250 mg - Filmtabletten Sweden (SE)
许可日期	2002/01/16
最近更新日期	2022/05/06
药物ATC编码	J01MA02 ciprofloxacin
申请类型	TypeLevel1：Abridged TypeLevel2：Initial Application TypeLevel3：Generic Article 4.8(a)(iii), first paragraph TypeLevel4：Chemical Substance TypeLevel5：Prescription Only
附件文件下载	Final SPC \| 1.3.1 spc-label-pl - common-spc - 11,817Date of last change:2021/06/04 Final PL \| 1.3.1 spc-label-pl - common-pl - 12,296Date of last change:2021/06/04 Final Product Information \| 1.3.1 spc-label-pl - common-spc - 9,603 cleanDate of last change:2019/03/29 Final Product Information \| 1.3.1 spc-label-pl - common-pl - 10,157 cleanDate of last change:2019/03/29 Final Labelling \| Final common labelling text Ciprofloxacin Sandoz NLH0301-0303-0305Date of last change:2018/09/17
市场状态	Positive