欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DE/H/3385/004
药品名称
Liprimar 80 mg
活性成分
Atorvastatin 80.0 mg
剂型
Film-coated tablet
上市许可持有人
Viatris Pharma GmbH Lütticher Str. 5 53842 Troisdorf Germany
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
Italy (IT)
Finland (FI)
许可日期
2011/10/20
最近更新日期
2025/01/29
药物ATC编码
C10AA05 atorvastatin
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 Product Information
|
final_common_PI_DE_H_3385_001_004_IA_058_G
Date of last change:2024/11/28
Final PL
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apz 021 SuppDoc m1_3_1_de_h_0109_001_004
Date of last change:2024/09/06
Final SPC
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apz 021 SuppDoc m1_3_1_de_h_0109_001_004_2
Date of last change:2024/09/06
Final PL
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apz 021 SuppDoc m1_3_1_de_h_0109_005_008
Date of last change:2024/09/06
Final SPC
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apz 021 SuppDoc m1_3_1_de_h_0109_005_008_2
Date of last change:2024/09/06
Final PL
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apz 021 SuppDoc m1_3_1_de_h_2958_2959_001_004
Date of last change:2024/09/06
Final SPC
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apz 021 SuppDoc m1_3_1_de_h_2958_2959_001_004_2
Date of last change:2024/09/06
Final PL
|
apz 021 SuppDoc m1_3_1_de_h_3384_001_004
Date of last change:2024/09/06
Final SPC
|
apz 021 SuppDoc m1_3_1_de_h_3384_001_004_2
Date of last change:2024/09/06
Final PL
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apz 021 SuppDoc m1_3_1_de_h_3384_005_008
Date of last change:2024/09/06
Final SPC
|
apz 021 SuppDoc m1_3_1_de_h_3384_005_008_2
Date of last change:2024/09/06
Final PL
|
apz 021 SuppDoc m1_3_1_de_h_3385_001_004
Date of last change:2024/09/06
Final SPC
|
apz 021 SuppDoc m1_3_1_de_h_3385_001_004_2
Date of last change:2024/09/06
Final PL
|
apz 021 SuppDoc m1_3_1_de_h_3616_001_004
Date of last change:2024/09/06
Final SPC
|
apz 021 SuppDoc m1_3_1_de_h_3616_001_004_2
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase