欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/2386/002
药品名称
Aktiprol
活性成分
amisulpride 100.0 mg
剂型
Tablet
上市许可持有人
Medichemie Ltd. 1-10 Constantinoupoleos Street 3011 Limassol Cyprus
参考成员国 - 产品名称
Denmark (DK)
Aktiprol
互认成员国 - 产品名称
Greece (GR)
AKTIPROL
Latvia (LV)
Aktiprol 100 mg tabletes
Cyprus (CY)
AKTRIPROL TABS
Malta (MT)
许可日期
2015/04/20
最近更新日期
2023/01/03
药物ATC编码
N05AL05 amisulpride
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Labelling
|
2386 common_labelling_v1_2_clean
Date of last change:2024/09/06
Final PL
|
common_pil_march2015_v1_3_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_feb2015_v1_2_clean
Date of last change:2024/09/06
PubAR
|
Final PAR Aktiprol DKH2386_001_004_DC
Date of last change:2024/09/06
PubAR Summary
|
Final sPAR Aktiprol DKH2386_001_004_DC
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase