欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
NL/H/1450/001
药品名称
Ibagenit 150 mg
活性成分
ibandronic acid 150.0 mg
剂型
Film-coated tablet
上市许可持有人
Mylan BV Dieselweg25, 3752 LB Bunschoten 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
2009/07/21
最近更新日期
2015/12/01
药物ATC编码
M05BA06 ibandronic acid
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 PL
|
common_pl_nl1446v008clean
Date of last change:2024/09/06
Final PL
|
common_pl_nl1446v008highlighted
Date of last change:2024/09/06
Final PL
|
common_pl_nl1447v007clean
Date of last change:2024/09/06
Final PL
|
common_pl_nl1447v007highlighted
Date of last change:2024/09/06
Final PL
|
common_pl_nl1449v008clean
Date of last change:2024/09/06
Final PL
|
common_pl_nl1449v008highlighted
Date of last change:2024/09/06
Final PL
|
common_pl_nl1450v007clean
Date of last change:2024/09/06
Final PL
|
common_pl_nl1450v007highlighted
Date of last change:2024/09/06
Final SPC
|
common_spc_nl1446v008clean
Date of last change:2024/09/06
Final SPC
|
common_spc_nl1446v008highlighted
Date of last change:2024/09/06
Final SPC
|
common_spc_nl1447v007clean
Date of last change:2024/09/06
Final SPC
|
common_spc_nl1447v007highlighted
Date of last change:2024/09/06
Final SPC
|
common_spc_nl1449v008clean
Date of last change:2024/09/06
Final SPC
|
common_spc_nl1449v008highlighted
Date of last change:2024/09/06
Final SPC
|
common_spc_nl1450v007clean
Date of last change:2024/09/06
Final SPC
|
common_spc_nl1450v007highlighted
Date of last change:2024/09/06
PubAR
|
PAR_1450_DC_18 Aug 2010
Date of last change:2024/09/06
市场状态
Withdrawn（注：已撤市）
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European Union HMA Authorisation of Medicines DataBase