欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
DE/H/1110/003
药品名称
Pramipexol STADA 0,35 mg Tabletten
活性成分
pramipexole dihydrochloride 0.5 mg
剂型
Tablet
上市许可持有人
Stadapharm GmbH Stadastr. 2-18 61118 Bad Vilbel Germany
参考成员国 - 产品名称
Germany (DE)
互认成员国 - 产品名称
Sweden (SE)
Emwepel
许可日期
2008/12/04
最近更新日期
2024/03/04
药物ATC编码
N04BC05 pramipexole
申请类型
TypeLevel1：
Abridged
TypeLevel2：
Additional Strength/Form
TypeLevel3：
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4：
Chemical Substance
TypeLevel5：
Prescription Only
附件文件下载
Final SPC
|
final_common_spc_DE_H_1110_001_004_IA_038
Date of last change:2024/03/04
Final PL
|
final_common_pl_DE_H_1110_001_004_IA_038
Date of last change:2024/03/04
Final Product Information
|
final-common-PL-1110-033
Date of last change:2020/06/10
Final Product Information
|
final-common-SPC-1110-033
Date of last change:2020/06/10
Final Labelling
|
DE1110_Pramipexol_Lab-inner-0.7mg_20131031_renewal
Date of last change:2013/10/31
Final Labelling
|
DE1110_Pramipexol_Lab-inner-0.35mg_20131031_renewal
Date of last change:2013/10/31
Final Labelling
|
DE1110_Pramipexol_Lab-inner-0.088mg_20131031_renewal
Date of last change:2013/10/31
Final Labelling
|
DE1110_Pramipexol_Lab-inner-1.1mg_20131031_renewal
Date of last change:2013/10/31
Final Labelling
|
DE1110_Pramipexol_Lab--outer-0.7mg_20131031_renewal
Date of last change:2013/10/31
Final Labelling
|
DE1110_Pramipexol_Lab-outer-0.18mg_20131031_renewal
Date of last change:2013/10/31
Final Labelling
|
DE1110_Pramipexol_Lab-outer-0.35mg_20131031_renewal
Date of last change:2013/10/31
Final Labelling
|
DE1110_Pramipexol_Lab-outer-1.1mg_20131031_renewal
Date of last change:2013/10/31
Final Labelling
|
DE1110_Pramipexol-Lab-inner-0.18mg_20131031_renewal
Date of last change:2013/10/31
Final Labelling
|
DE1110_Pramipexol-Lab-outer-0.088mg_20131031_renewal
Date of last change:2013/10/31
市场状态
Positive
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