欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1115/004
药品名称
Risperidona SVUS
活性成分
risperidone 4.0 mg
剂型
Film-coated tablet
上市许可持有人
SVUS
参考成员国 - 产品名称
Portugal (PT)
Risperidona SVUS
互认成员国 - 产品名称
Poland (PL)
Risperidone Farmax
Hungary (HU)
许可日期
2014/09/23
最近更新日期
2018/11/30
药物ATC编码
N05AX08 risperidone
申请类型
TypeLevel1:
Abridged
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
|
573700_573805_573808_573807_20141117_PAR_GBB
Date of last change:2024/09/06
Final Product Information
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common_impack
Date of last change:2024/09/06
Final Product Information
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common_outer_1mg
Date of last change:2024/09/06
Final Product Information
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common_outer_2mg
Date of last change:2024/09/06
Final Product Information
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common_outer_3mg
Date of last change:2024/09/06
Final Product Information
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common_outer_4mg
Date of last change:2024/09/06
Final Product Information
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common_spc_clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase