欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/0326/001
药品名称
Azathioprine 25 mg
活性成分
azathioprine 25.0 mg
剂型
Film-coated tablet
上市许可持有人
Hexal AG Industriestrasse 25 83607 Holzkirchen Germany
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Germany (DE)
United Kingdom (Northern Ireland) (XI)
许可日期
2002/07/08
最近更新日期
2023/11/02
药物ATC编码
L04AX01 azathioprine
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Generic Article 4.8(a)(iii), first paragraph
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Product Information
|
1.3.1 spc-label-pl - common-pl-001 - 62
Date of last change:2021/09/03
Final Product Information
|
1.3.1 spc-label-pl - common-pl-002 - 69
Date of last change:2021/09/03
Final Product Information
|
1.3.1 spc-label-pl - common-spc - 12,460
Date of last change:2021/09/03
Final SPC
|
common-spc-clean
Date of last change:2020/09/10
Final PL
|
common-pl-clean
Date of last change:2020/09/10
Final Labelling
|
1.3.1 spc-label-pl - common-outer-001ia034 - 4 - clean version
Date of last change:2019/04/01
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase