欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0100/001
药品名称
MIRENA
活性成分
Levonorgestrel 52.0 mg
剂型
Intrauterine device
上市许可持有人
Bayer Schering Pharma Oy
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Spain (ES)
Poland (PL)
许可日期
2000/03/02
最近更新日期
2024/09/16
药物ATC编码
G03AC03 levonorgestrel
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
|
EU_PL Mirena _en__valid as per 20 March 2023
Date of last change:2024/09/06
Final SPC
|
Mirena_EU_MRP_SmPC_proposed_D80_annotated_final
Date of last change:2024/09/06
Final Labelling
|
MRP_PT100_IA_insertion instruction_25 Jan11_highlighted_approved
Date of last change:2024/09/06
市场状态
Positive
©2006-2024
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European Union HMA Authorisation of Medicines DataBase