欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/3047/001
药品名称
Imodium Plus Caplets
活性成分
loperamide hydrochloride 2.0 mg
剂型
Tablet
上市许可持有人
Mcneil Denmark ApS Transformervej 14 2860 Søborg Denmark
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
Germany (DE)
Belgium (BE)
Imodium Duo 2 mg/125 mg tabletten
Netherlands (NL)
Luxembourg (LU)
Ireland (IE)
France (FR)
Spain (ES)
Portugal (PT)
Sweden (SE)
Norway (NO)
Finland (FI)
Slovakia (SK)
Greece (GR)
Hungary (HU)
IMODIUM PLUS 2 mg/125 mg tabletta
Bulgaria (BG)
Imodium Plus
Cyprus (CY)
Czechia (CZ)
Imodium Plus
Romania (RO)
许可日期
2008/04/05
最近更新日期
2024/06/18
药物ATC编码
A07DA53 loperamide, combinations
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
Final SPC
|
Common_SmPC_IMODIUM PLUS_DK_H_3047_clean
Date of last change:2024/09/06
Final Product Information
|
Imodium Plus_PI_clean
Date of last change:2024/09/06
Final PL
|
Imodium Plus_PI_clean__
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase