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

MR编号	NL/H/2124/002
药品名称	Ibandronic acid ratiopharm 6 mg
活性成分	ibandronic acid 6.0 mg
剂型	Concentrate for solution for infusion
上市许可持有人	ratiopharm Nederland BV Florapark 4 2012 HK Haarlem The Netherlands
参考成员国 - 产品名称	Netherlands (NL)
互认成员国 - 产品名称
许可日期	2011/12/23
最近更新日期	2023/01/17
药物ATC编码	M05BA06 ibandronic acid
申请类型	TypeLevel1：Abridged TypeLevel2：Multiple (Copy) 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 \| Common Label 2 mgDate of last change:2024/09/06 Final Product Information \| Common Label 3 mgDate of last change:2024/09/06 Final Product Information \| Common Label 6 mgDate of last change:2024/09/06 Final Labelling \| Ibandronic acid 2_6 mg concentrate for solution for injection_Outer Carton_trackedDate of last change:2024/09/06 Final Product Information \| Ibandronic acid_NL_H_2124_001_002_SmPC_03_06_20Date of last change:2024/09/06 Final SPC \| Ibandronic acid_NL_H_2124_001_002_SmPC_08_04_21Date of last change:2024/09/06 Final Product Information \| Ibandronic acid_NL_H_2124_001_PIL_03_06_20Date of last change:2024/09/06 Final PL \| Ibandronic acid_NL_H_2124_001_PIL_08_04_21Date of last change:2024/09/06 Final Product Information \| Ibandronic acid_NL_H_2124_002_PIL_03_06_20Date of last change:2024/09/06 Final PL \| Ibandronic acid_NL_H_2124_002_PIL_08_04_21Date of last change:2024/09/06 Final Product Information \| Ibandronic acid_NL_H_2124_003_PIL_03_06_20Date of last change:2024/09/06 Final Product Information \| Ibandronic acid_NL_H_2124_003_SmPC_03_06_20Date of last change:2024/09/06 PubAR \| PAR_2124_DC_Ibandroninezuur_26 sept 2012Date of last change:2024/09/06
市场状态	Withdrawn（注：已撤市）