欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
BG/H/0111/001
药品名称
Bilamcar 8mg/5mg
活性成分
AMLODIPINE BESILATE 5.0 mg
candesartancilexetil 8.0 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 8 mg/5 mg Hartkapseln
Portugal (PT)
Greece (GR)
Czechia (CZ)
Bilamcar 8mg / 5mg
Romania (RO)
Slovakia (SK)
Bilamcar
许可日期
2018/10/15
最近更新日期
2024/11/12
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 SPC
|
common_lbl_16mg_10mg_clean
Date of last change:2024/09/06
Final PL
|
common_lbl_16mg_10mg_clean_210_OK
Date of last change:2024/09/06
Final SPC
|
common_lbl_16mg_10mg_track
Date of last change:2024/09/06
Final SPC
|
common_lbl_16mg_5mg_clean
Date of last change:2024/09/06
Final PL
|
common_lbl_16mg_5mg_clean_210_OK
Date of last change:2024/09/06
Final SPC
|
common_lbl_16mg_5mg_track
Date of last change:2024/09/06
Final SPC
|
common_lbl_8mg_10mg_clean
Date of last change:2024/09/06
Final PL
|
common_lbl_8mg_10mg_clean_210_OK
Date of last change:2024/09/06
Final SPC
|
common_lbl_8mg_10mg_track
Date of last change:2024/09/06
Final SPC
|
common_lbl_8mg_5mg_clean
Date of last change:2024/09/06
Final PL
|
common_lbl_8mg_5mg_clean_210_OK
Date of last change:2024/09/06
Final SPC
|
common_lbl_8mg_5mg_track
Date of last change:2024/09/06
Final SPC
|
common_pl_clean
Date of last change:2024/09/06
Final PL
|
common_pl_clean_210_OK
Date of last change:2024/09/06
Final Product Information
|
common_pl_clean_4
Date of last change:2024/09/06
Final SPC
|
common_pl_track
Date of last change:2024/09/06
Final Product Information
|
common_pl_track_4
Date of last change:2024/09/06
Final SPC
|
common_smpc_clean
Date of last change:2024/09/06
Final PL
|
common_smpc_clean_210_OK
Date of last change:2024/09/06
Final Product Information
|
common_smpc_clean_4
Date of last change:2024/09/06
Final SPC
|
common_smpc_track
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
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European Union HMA Authorisation of Medicines DataBase