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 |
2021/11/18 |
SUPPL-19(补充) |
Approval |
Labeling |
STANDARD
;Orphan
|
|
|
2021/02/24 |
SUPPL-18(补充) |
Approval |
Labeling |
STANDARD
;Orphan
|
|
|
2019/12/19 |
SUPPL-17(补充) |
Approval |
Labeling |
STANDARD
;Orphan
|
|
|
2017/09/29 |
SUPPL-15(补充) |
Approval |
Labeling |
STANDARD
;Orphan
|
|
|
2016/10/13 |
SUPPL-13(补充) |
Approval |
Labeling |
STANDARD
;Orphan
|
|
|
2014/09/30 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
;Orphan
|
|
|
2014/08/22 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2013/06/18 |
SUPPL-8(补充) |
Approval |
REMS |
N/A
|
|
|
2013/01/22 |
SUPPL-6(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2012/12/21 |
SUPPL-7(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2012/07/20 |
SUPPL-4(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2012/07/20 |
SUPPL-3(补充) |
Approval |
Labeling |
PRIORITY
|
|
|
2011/11/17 |
SUPPL-2(补充) |
Approval |
REMS |
N/A
|
|
|
2010/01/22 |
ORIG-1(原始申请) |
Approval |
Type 1 - New Molecular Entity |
PRIORITY
;Orphan
|
|
|
与本品相关的专利信息(来自FDA橙皮书Orange Book)
与本品治疗等效的药品
活性成分:DALFAMPRIDINE 剂型/给药途径:TABLET, EXTENDED RELEASE;ORAL 规格:10MG 治疗等效代码:AB
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 |
022250 |
001 |
NDA |
AMPYRA |
DALFAMPRIDINE |
TABLET, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
Yes |
Yes |
AB |
2010/01/22
|
MERZ PHARMS |
206811 |
001 |
ANDA |
DALFAMPRIDINE |
DALFAMPRIDINE |
TABLET, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2017/01/23
|
AUROBINDO PHARMA |
206836 |
001 |
ANDA |
DALFAMPRIDINE |
DALFAMPRIDINE |
TABLET, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2017/01/23
|
ACTAVIS LABS FL INC |
206863 |
001 |
ANDA |
DALFAMPRIDINE |
DALFAMPRIDINE |
TABLET, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2018/07/11
|
ACCORD HLTHCARE |
206765 |
001 |
ANDA |
DALFAMPRIDINE |
DALFAMPRIDINE |
TABLET, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2018/07/30
|
ALKEM LABS LTD |
206646 |
001 |
ANDA |
DALFAMPRIDINE |
DALFAMPRIDINE |
TABLET, EXTENDED RELEASE;ORAL |
10MG |
Discontinued |
No |
No |
AB |
2018/10/24
|
HIKMA |
210158 |
001 |
ANDA |
DALFAMPRIDINE |
DALFAMPRIDINE |
TABLET, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2019/03/11
|
MICRO LABS |
208292 |
001 |
ANDA |
DALFAMPRIDINE |
DALFAMPRIDINE |
TABLET, EXTENDED RELEASE;ORAL |
10MG |
Prescription |
No |
No |
AB |
2019/05/21
|
SUN PHARM |