欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PT/H/1253/001
药品名称
Deferiprone Genepharm
活性成分
deferiprone 500.0 mg
剂型
Film-coated tablet
上市许可持有人
Genepharm, S.A
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Greece (GR)
BEFEPROX (ex FORCEMA)
许可日期
2015/05/25
最近更新日期
2023/10/14
药物ATC编码
V03AC02 deferiprone
申请类型
TypeLevel1：
Known Active Substance
TypeLevel2：
Initial Application
TypeLevel3：
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4：
Chemical Substance
TypeLevel5：
Prescription Only
附件文件下载
PubAR
|
585424_585425_20151022_PAR_IRS
Date of last change:2024/09/06
Final Product Information
|
common_impack_1000mg
Date of last change:2024/09/06
Final Product Information
|
common_impack_500mg
Date of last change:2024/09/06
Final Product Information
|
common_outer_1000 mg
Date of last change:2024/09/06
Final Product Information
|
common_outer_500mg
Date of last change:2024/09/06
Final Product Information
|
common_pl_combined
Date of last change:2024/09/06
Final Product Information
|
common_spc_1000mg_v1
Date of last change:2024/09/06
Final Product Information
|
common_spc_500mg_v1
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase