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
>>>原始批准或临时批准<<<
| 审批日期 | 提交号 | 审批结论 | 提交分类 | 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 |
| 1996/08/05 |
ORIG-1(原始申请) |
Approval |
Type 1 - New Molecular Entity |
STANDARD
|
|
|
>>>补充申请<<<
| 审批日期 | 提交号 | 审批结论 | 补充类别或审批类型 | 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 |
| 2022/04/28 |
SUPPL-46(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2021/12/02 |
SUPPL-45(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2021/02/16 |
SUPPL-42(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2020/01/28 |
SUPPL-40(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2019/07/12 |
SUPPL-39(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2017/10/31 |
SUPPL-38(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2017/10/31 |
SUPPL-37(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2017/03/10 |
SUPPL-36(补充) |
Approval |
Labeling-Container/Carton Labels |
STANDARD
|
|
|
| 2017/03/01 |
SUPPL-3(补充) |
Approval |
Efficacy-New Patient Population |
STANDARD
|
|
|
| 2016/11/04 |
SUPPL-33(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2016/06/16 |
SUPPL-31(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2016/06/01 |
SUPPL-30(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2016/03/03 |
SUPPL-29(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2015/06/04 |
SUPPL-28(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2014/06/12 |
SUPPL-25(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2014/06/09 |
SUPPL-26(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2014/01/03 |
SUPPL-23(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2013/10/22 |
SUPPL-24(补充) |
Approval |
Labeling-Container/Carton Labels |
STANDARD
|
|
|
| 2013/08/30 |
SUPPL-21(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2013/03/06 |
SUPPL-20(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2011/11/13 |
SUPPL-19(补充) |
Approval |
Labeling-Package Insert |
UNKNOWN
|
|
|
| 2011/11/13 |
SUPPL-16(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2011/11/13 |
SUPPL-9(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2011/11/13 |
SUPPL-8(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2002/01/02 |
SUPPL-7(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2001/08/13 |
SUPPL-5(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2001/08/13 |
SUPPL-4(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 1998/11/20 |
SUPPL-2(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 1996/12/26 |
SUPPL-1(补充) |
Approval |
Labeling |
STANDARD
|
|
|
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 |
| 001 |
4925860 |
2007/08/05 |
|
|
|
|
|
PDF格式 | **本条是由Drugfuture回溯的历史信息** |
与本品治疗等效的药品
>>>活性成分:FOSPHENYTOIN SODIUM; 剂型/给药途径:INJECTABLE;INJECTION; 规格:EQ 50MG PHENYTOIN NA/ML; 治疗等效代码:AP<<<
| 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 |
| 020450 |
001 |
NDA |
CEREBYX |
FOSPHENYTOIN SODIUM |
INJECTABLE;INJECTION |
EQ 50MG PHENYTOIN NA/ML |
Prescription |
Yes |
Yes |
AP |
1996/08/05
|
PARKE DAVIS |
| 077481 |
001 |
ANDA |
FOSPHENYTOIN SODIUM |
FOSPHENYTOIN SODIUM |
INJECTABLE;INJECTION |
EQ 50MG PHENYTOIN NA/ML |
Prescription |
No |
No |
AP |
2007/08/06
|
HIKMA |
| 077989 |
001 |
ANDA |
FOSPHENYTOIN SODIUM |
FOSPHENYTOIN SODIUM |
INJECTABLE;INJECTION |
EQ 50MG PHENYTOIN NA/ML |
Prescription |
No |
No |
AP |
2007/08/06
|
HIKMA |
| 078052 |
001 |
ANDA |
FOSPHENYTOIN SODIUM |
FOSPHENYTOIN SODIUM |
INJECTABLE;INJECTION |
EQ 50MG PHENYTOIN NA/ML |
Prescription |
No |
No |
AP |
2007/08/06
|
FRESENIUS KABI USA |
| 078137 |
001 |
ANDA |
FOSPHENYTOIN SODIUM |
FOSPHENYTOIN SODIUM |
INJECTABLE;INJECTION |
EQ 50MG PHENYTOIN NA/ML |
Prescription |
No |
No |
AP |
2007/08/06
|
WOCKHARDT BIO AG |
| 078417 |
001 |
ANDA |
FOSPHENYTOIN SODIUM |
FOSPHENYTOIN SODIUM |
INJECTABLE;INJECTION |
EQ 50MG PHENYTOIN NA/ML |
Prescription |
No |
No |
AP |
2008/03/18
|
SUN PHARM |
| 078765 |
001 |
ANDA |
FOSPHENYTOIN SODIUM |
FOSPHENYTOIN SODIUM |
INJECTABLE;INJECTION |
EQ 50MG PHENYTOIN NA/ML |
Prescription |
No |
No |
AP |
2009/12/02
|
HIKMA FARMACEUTICA |
| 078736 |
001 |
ANDA |
FOSPHENYTOIN SODIUM |
FOSPHENYTOIN SODIUM |
INJECTABLE;INJECTION |
EQ 50MG PHENYTOIN NA/ML |
Discontinued |
No |
No |
AP |
2010/06/08
|
PHARMOBEDIENT |
| 214926 |
001 |
ANDA |
FOSPHENYTOIN SODIUM |
FOSPHENYTOIN SODIUM |
INJECTABLE;INJECTION |
EQ 50MG PHENYTOIN NA/ML |
Prescription |
No |
No |
AP |
2023/10/13
|
GLAND |