欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
IE/H/1178/002
药品名称
Midodrine 5mg Tablets
活性成分
Midodrine 5.0 mg
剂型
Tablet
上市许可持有人
Morningside Malta Ltd 93 Mill Street Qormi QRM 3102 Malta
参考成员国 - 产品名称
Ireland (IE)
互认成员国 - 产品名称
Denmark (DK)
Sweden (SE)
Midodrine Hydrochloride Morningside
Norway (NO)
许可日期
2022/07/20
最近更新日期
2024/11/19
药物ATC编码
C01CA17 midodrine
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
Final PL
|
Common Label_m131_leaflet_common_v1
Date of last change:2024/09/06
Final SPC
|
Final SPC _spc_common
Date of last change:2024/09/06
PubAR
|
Public_AR_PA23142_008_002_19032024161736
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase