欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
NL/H/0490/001
药品名称
Domperidon Sandoz 10 mg
活性成分
domperidone maleate 10.0 mg
剂型
Tablet
上市许可持有人
Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
许可日期
2004/06/15
最近更新日期
2024/03/26
药物ATC编码
A03FA03 domperidone
申请类型
TypeLevel1：
Known Active Substance
TypeLevel2：
Initial Application
TypeLevel3：
Informed Constent Article 4.8 (a)i
TypeLevel4：
Chemical Substance
TypeLevel5：
Non Prescription (including OTC)
附件文件下载
Final Product Information
|
1_3_1 spc_label_pl _ common_outer _ 4_253
Date of last change:2024/09/06
Final Labelling
|
1_3_1 spc_label_pl _ common_outer _ 4_253 clean
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_pl _ 8_876
Date of last change:2024/09/06
Final Labelling
|
1_3_1 spc_label_pl _ common_pl _ 8_876 clean
Date of last change:2024/09/06
Final Product Information
|
1_3_1 spc_label_pl _ common_spc _ 8_311
Date of last change:2024/09/06
Final Labelling
|
1_3_1 spc_label_pl _ common_spc _ 8_311 clean
Date of last change:2024/09/06
Final PL
|
common_pl
Date of last change:2024/09/06
Final SPC
|
common_spc
Date of last change:2024/09/06
市场状态
Withdrawn（注：已撤市）
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European Union HMA Authorisation of Medicines DataBase