欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
AT/H/1049/002
药品名称
Rosuvastatin "Ratiopharm"
活性成分
Rosuvastatin calcium 10.0 mg
剂型
Film-coated tablet
上市许可持有人
Teva B.V. Swensweg 5 2031 GA The Netherlands
参考成员国 - 产品名称
Austria (AT)
互认成员国 - 产品名称
Spain (ES)
Portugal (PT)
Finland (FI)
Rosuvastatin ratiopharm
Czechia (CZ)
Rosuvastatin-ratiopharm 10 mg
Iceland (IS)
Norway (NO)
Bulgaria (BG)
Rosuvastatin Teva
许可日期
2010/11/02
最近更新日期
2024/11/22
药物ATC编码
C10AA07 rosuvastatin
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
PubAR
|
AT_H_1049_001_004_PAR
Date of last change:2024/09/06
Final SPC
|
final_common_SmPC_AT_H_1050_001_002_IB_031_clean
Date of last change:2024/09/06
Final Labelling
|
final_LAB_AT_H_1049_001_004_P_001_clean
Date of last change:2024/09/06
Final PL
|
final_PL_AT_H_1049_001_004_P_001_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_clean
Date of last change:2024/09/06
Final Product Information
|
common_spc_clean
Date of last change:2024/09/06
PubAR Summary
|
Summary_PAR_Rouvastatin Ratiopharm_DKH1772_001_004_DC_update
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase