批准日期,申请提交历史,通知信,药品说明书,审评文件等信息
提交状态日期 | 提交号 | 审批结论 | 申请内容分类 | 审评优先级;罕用药状态 | 通知信、审评文件、说明书、包装标签 | 备注 |
2023/10/13 |
SUPPL-3(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2022/02/25 |
SUPPL-2(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2022/02/15 |
SUPPL-1(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/03/16 |
ORIG-1(原始申请) |
Approval |
|
|
|
|
与本品相关的专利信息(来自FDA橙皮书Orange Book)
关联产品号 | 专利号 | 专利过期日 | 是否物质专利 | 是否产品专利 | 专利用途代码 | 撤销请求 | 提交日期 | 专利下载 | 备注 |
无 |
与本品治疗等效的药品
活性成分:DEXTROAMPHETAMINE SULFATE 剂型/给药途径:TABLET;ORAL 规格:5MG 治疗等效代码:AA
申请号 | 产品号 | 申请类型 | 商品名 | 活性成分 | 剂型/给药途径 | 规格 | 市场状态 | RLD | RS | TE Code | 产品号批准日期 | 申请人 |
040361 |
001 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AA |
2001/01/31
|
BARR |
040436 |
001 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AA |
2002/01/29
|
SPECGX LLC |
090533 |
002 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AA |
2011/10/25
|
AZURITY |
202893 |
001 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AA |
2013/07/31
|
AUROLIFE PHARMA LLC |
203548 |
001 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AA |
2015/11/23
|
AVANTHI INC |
204330 |
001 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AA |
2016/03/16
|
NOVEL LABS INC |
210059 |
001 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AA |
2017/10/18
|
NUVO PHARM |
212160 |
002 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
Prescription |
No |
No |
AA |
2021/06/07
|
WINDER LABS LLC |
206095 |
001 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
5MG |
Discontinued |
No |
No |
AA |
2022/08/18
|
TRIS PHARMA INC |
活性成分:DEXTROAMPHETAMINE SULFATE 剂型/给药途径:TABLET;ORAL 规格:10MG 治疗等效代码:AA
申请号 | 产品号 | 申请类型 | 商品名 | 活性成分 | 剂型/给药途径 | 规格 | 市场状态 | RLD | RS | TE Code | 产品号批准日期 | 申请人 |
040361 |
002 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
Prescription |
No |
Yes |
AA |
2001/01/31
|
BARR |
040436 |
002 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AA |
2002/01/29
|
SPECGX LLC |
090533 |
004 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AA |
2011/10/25
|
AZURITY |
202893 |
002 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AA |
2013/07/31
|
AUROLIFE PHARMA LLC |
203548 |
002 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AA |
2015/11/23
|
AVANTHI INC |
204330 |
002 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AA |
2016/03/16
|
NOVEL LABS INC |
210059 |
002 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AA |
2017/10/18
|
NUVO PHARM |
212160 |
004 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
Prescription |
No |
No |
AA |
2021/06/07
|
WINDER LABS LLC |
206095 |
002 |
ANDA |
DEXTROAMPHETAMINE SULFATE |
DEXTROAMPHETAMINE SULFATE |
TABLET;ORAL |
10MG |
Discontinued |
No |
No |
AA |
2022/08/18
|
TRIS PHARMA INC |