欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/0160/001
药品名称
Atenolol 50 Sandoz
活性成分
atenolol 50.0 mg
剂型
Tablet
上市许可持有人
Sandoz BV Almere, The Netherlands
参考成员国 - 产品名称
Netherlands (NL)
Atenolol
互认成员国 - 产品名称
Denmark (DK)
Belgium (BE)
Sweden (SE)
Finland (FI)
许可日期
1999/06/23
最近更新日期
2022/01/24
药物ATC编码
C07AB03 atenolol
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Bibliographic Article 4.8 (a) (ii)
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
1.3.1 spc-label-pl - common-pl-cl - 987
Date of last change:2019/10/17
Final SPC
|
1.3.1 spc-label-pl - common-spc-cl - 898
Date of last change:2019/10/17
Final Labelling
|
1.3.1 spc-label-pl - common-outer-cl - 458
Date of last change:2019/10/17
Final Product Information
|
common-outer-clean
Date of last change:2014/10/30
Final Product Information
|
common-pl-clean
Date of last change:2014/10/30
Final Product Information
|
common-spc-clean
Date of last change:2014/10/30
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase