欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1668/001
药品名称
AMSALYO
活性成分
Amsacrine 75.0 mg
剂型
Powder for concentrate for solution for infusion
上市许可持有人
Eurocept International bv, Netherlands
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Italy (IT)
Croatia (HR)
Amlyo 75 mg prašak za koncentrat za otopinu za infuziju
Norway (NO)
Finland (FI)
Germany (DE)
AMSALYO 75 mg Pulver für ein Konzentrat zur Herstellung einer Infusionslösung
Poland (PL)
Denmark (DK)
Slovakia (SK)
Netherlands (NL)
Luxembourg (LU)
Iceland (IS)
Ireland (IE)
Austria (AT)
Belgium (BE)
许可日期
2018/04/26
最近更新日期
2025/02/06
药物ATC编码
L01XX01 amsacrine
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Bibliographic Art 10 a Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
SE_H_1668_001_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_1668_001_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_1668_001_PAR
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase