欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/0453/001
药品名称
Paroxetine 40 mg, tablets
活性成分
paroxetine hydrochloride 40.0 mg
剂型
Tablet
上市许可持有人
Ratiopharm GmbH Graf-Arco-Strasse 3 89079 Ulm Germany
参考成员国 - 产品名称
Netherlands (NL)
RVG 33151
互认成员国 - 产品名称
Austria (AT)
Paroxetin-ratiopharm 40 mg Tabletten
许可日期
2006/10/04
最近更新日期
2024/04/08
药物ATC编码
N06AB05 paroxetine
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Multiple (Copy) Application
TypeLevel3:
Other Generic application Art 10.3 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Product Information
|
common_interpack_clean
Date of last change:2024/09/06
Final Product Information
|
common_outer_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_clean
Date of last change:2024/09/06
Final Product Information
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common_spc_clean
Date of last change:2024/09/06
Final PL
|
Final PL
Date of last change:2024/09/06
Final SPC
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Final SmPC
Date of last change:2024/09/06
Final Labelling
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Paroxetine 40 mg tablets_OuP_NL_H_453_001_23_04_18
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase