欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0663/001
药品名称
Moapar
活性成分
Triptorelin 11.25 mg
剂型
Powder and solvent for prolonged-release suspension for injection
上市许可持有人
Medipha Santé , France
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Ireland (IE)
Greece (GR)
SALVACYL
Austria (AT)
Poland (PL)
Salvacyl
Germany (DE)
Belgium (BE)
Netherlands (NL)
United Kingdom (Northern Ireland) (XI)
France (FR)
许可日期
2007/03/06
最近更新日期
2025/02/10
药物ATC编码
L02AE04 triptorelin
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Full Dossier Art 8.3(i) Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
SE_H_0663_001_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_0663_001_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_0663_001_PAR
Date of last change:2024/09/06
Final Product Information
|
common_combined_spc_pi_3point75mg_annotated
Date of last change:2024/09/06
市场状态
Positive
©2006-2025
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European Union HMA Authorisation of Medicines DataBase