欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
BG/H/0111/004
药品名称
Bilamcar 16mg/10mg
活性成分
AMLODIPINE BESILATE 10.0 mg
candesartancilexetil 16.0 mg
剂型
Capsule, hard
上市许可持有人
Swyssi AG 14 Lyoner Strasse Frankfurt am Main 60528 Germany
参考成员国 - 产品名称
Bulgaria (BG)
Bilamcar
互认成员国 - 产品名称
Austria (AT)
Tilamcar 16 mg/10 mg Hartkapseln
Portugal (PT)
Greece (GR)
Czechia (CZ)
Bilamcar 16mg / 10 mg
Romania (RO)
Slovakia (SK)
许可日期
2018/10/15
最近更新日期
2025/08/15
药物ATC编码
C09DB07 candesartan and amlodipine
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Fixed combination Art 10b Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
common_pl_bilamcar_clean
Date of last change:2025/08/15
Final SPC
|
common_spc_bilamcar_clean
Date of last change:2025/08/15
Final Product Information
|
common_pl_clean_4
Date of last change:2024/09/06
Final Product Information
|
common_pl_track_4
Date of last change:2024/09/06
Final Product Information
|
common_smpc_clean_4
Date of last change:2024/09/06
Final Product Information
|
common_smpc_track_4
Date of last change:2024/09/06
市场状态
Positive
©2006-2025
Drugfuture
->
European Union HMA Authorisation of Medicines DataBase