欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/0650/001
药品名称
Azathioprin "Orifarm"
活性成分
azathioprine 50.0 mg
剂型
Film-coated tablet
上市许可持有人
Orifarm Generics A/S Energivej 15 5260 Odense S Denmark
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
Sweden (SE)
许可日期
2005/08/10
最近更新日期
2023/06/29
药物ATC编码
L04AX01 azathioprine
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
TypeLevel3:
Generic [Article 10.1.(a)(iii), first paragraph]
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Product Information
|
Azathioprin Orifarm TAB 20171212 SPC ENG A5154 CHJEN
Date of last change:2024/09/06
Final Product Information
|
Azathioprin Orifarm TAB 20180212 PIL ENG A5154 MABKE
Date of last change:2024/09/06
Final PL
|
Azathioprin Orifarm TAB 20210621 PIL ENG A6737 DOSRJ clean
Date of last change:2024/09/06
Final SPC
|
Azathioprin Orifarm TAB 20210621 SPC ENG A6737 DOSRJ clean
Date of last change:2024/09/06
Final Labelling
|
labelling
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase