欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/1656/001
药品名称
Nebivolol-ratiopharm 5 mg Tabletten
活性成分
nebivolol 5.0 mg
剂型
Tablet
上市许可持有人
ratiopharm GmbH Graf-Arco Str. 3 D-89079 Ulm
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
许可日期
2009/07/07
最近更新日期
2022/02/22
药物ATC编码
C07AB12 nebivolol
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
PAR
|
04_DE_1656_1_MR_Nebivolol_ratiopharm_final PAR
Date of last change:2023/01/17
Final Product Information
|
common-final-pl-1656-V017
Date of last change:2020/12/18
Final Product Information
|
common-final-spc-1656-V017
Date of last change:2020/12/18
Final SPC
|
common-pl-clean
Date of last change:2016/01/19
Final SPC
|
common-pl-tracked_2
Date of last change:2016/01/19
Final SPC
|
common-spc-clean_2
Date of last change:2016/01/19
Final SPC
|
common-spc-tracked_2
Date of last change:2016/01/19
Final PL
|
common-pl-clean
Date of last change:2016/01/19
Final PL
|
common-pl-tracked
Date of last change:2016/01/19
Final PL
|
common-spc-clean
Date of last change:2016/01/19
Final PL
|
common-spc-tracked
Date of last change:2016/01/19
市场状态
Withdrawn(注:已撤市)
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