欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
NL/H/0338/003
药品名称
Alprazolam-ratiopharm 1,0 mg
活性成分
alprazolam 1.0 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)
互认成员国 - 产品名称
Portugal (PT)
Germany (DE)
Austria (AT)
Alprazolam "ratiopharm" 1 mg-Tabletten
许可日期
2002/07/30
最近更新日期
2022/12/12
药物ATC编码
N05BA12 alprazolam
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Other Article 4.8(a)(iii), second paragraph
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
common_pl_0p25mg_clean
Date of last change:2024/09/06
Final PL
|
common_pl_0p5mg_clean
Date of last change:2024/09/06
Final PL
|
common_pl_1mg_clean
Date of last change:2024/09/06
Final Product Information
|
common_pl_cean combi
Date of last change:2024/09/06
Final SPC
|
common_spc_0p25mg_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_0p5mg_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_1mg_clean
Date of last change:2024/09/06
Final Labelling
|
outer_0_25 mg
Date of last change:2024/09/06
Final Labelling
|
outer_0_5 mg
Date of last change:2024/09/06
Final Labelling
|
outer_1_0 mg
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase