欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/6446/003
药品名称
Rosuvastatina Aurobindo
活性成分
Rosuvastatin calcium 20.0 mg
剂型
Film-coated tablet
上市许可持有人
Aurobindo Pharma (Portugal), Unip. Lda.
参考成员国 - 产品名称
Netherlands (NL)
互认成员国 - 产品名称
Finland (FI)
Romania (RO)
Rosuvastatina Aurobindo 20 mg comprimate filmate
Malta (MT)
Rosuvastatin Aurobindo 20mg Film coated tablets
Germany (DE)
Rosuvastatin Aurobindo 20 mg Filmtabletten
Belgium (BE)
Rosuvastatin AB 20mg filmomhulde tabletten
Luxembourg (LU)
France (FR)
Cyprus (CY)
ROSUVASTATIN AUROBINDO 20MG FC TABS
许可日期
2012/06/28
最近更新日期
2025/06/10
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 Summary
|
sPAR_NLH6446_Rosuvastatine Aurobindo 5 mg_ 10 mg_ 20 mg and 40 mg_13 August 2025_EN
Date of last change:2025/08/13
PubAR
|
PAR_NLH6446_Rosuvastatine Aurobindo 5 mg_ 10 mg_ 20 mg and 40 mg_13 August 2025
Date of last change:2025/08/13
Final PL
|
common_pl_clean
Date of last change:2024/10/28
Final Product Information
|
56412_56413_20130902_PAR_GBB
Date of last change:2024/09/06
Final Product Information
|
56414_56415_20130902_PAR_GBB
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase