欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/0803/001
药品名称
Nebivolol 5 mg
活性成分
Nebivolol 5.0 mg
剂型
Tablet
上市许可持有人
Centrafarm Services B.V. Nieuwe Donk 9 NL-4879 AC Etten-Leur The Netherlands
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Germany (DE)
Nebivolol STADA 5 mg Tabletten
Belgium (BE)
Luxembourg (LU)
Ireland (IE)
Austria (AT)
Nebovolol STADA 5 mg -Tabletten
France (FR)
Portugal (PT)
Italy (IT)
Latvia (LV)
Nemirostad 5 mg tablets
Lithuania (LT)
NEMIROSTAD 5 mg tabletės
Estonia (EE)
NEBILOSTAD
许可日期
2007/03/15
最近更新日期
2024/12/30
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
Final Labelling
|
1_3_1_Lab_outer_common_en_NL_H_0803_001_cl_Lable Common
Date of last change:2024/09/06
Final PL
|
1_3_1_PIL_common_NL_H_0803_001_cl
Date of last change:2024/09/06
Final SPC
|
1_3_1_SPC_common_NL_H_0803_001_cl
Date of last change:2024/09/06
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase