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 |
| 1991/09/27 |
ORIG-1(原始申请) |
Approval |
Type 1 - New Molecular Entity |
PRIORITY
|
|
|
>>>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 |
| 2020/10/28 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC)-Manufacturing Process |
N/A
|
|
|
| 2017/02/24 |
SUPPL-23(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2016/11/10 |
SUPPL-22(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2015/05/29 |
SUPPL-21(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 2014/11/07 |
SUPPL-20(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
| 2014/06/10 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 2012/02/10 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC) |
|
|
|
| 2007/11/27 |
SUPPL-17(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2006/05/15 |
SUPPL-16(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2000/06/13 |
SUPPL-14(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2000/06/13 |
SUPPL-13(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 1998/11/16 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC)-Control |
|
|
|
| 1997/03/31 |
SUPPL-9(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 1997/01/24 |
SUPPL-8(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 1997/01/24 |
SUPPL-7(补充) |
Approval |
Efficacy-New Dosing Regimen |
STANDARD
|
|
|
| 1997/01/24 |
SUPPL-6(补充) |
Approval |
Efficacy-New Indication |
STANDARD
|
|
|
| 1997/01/03 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC)-Control |
|
|
|
| 1995/12/12 |
SUPPL-2(补充) |
Approval |
Labeling |
|
|
|
| 1995/11/17 |
SUPPL-5(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 1995/06/16 |
SUPPL-3(补充) |
Approval |
Efficacy-New Indication |
UNKNOWN
|
|
|
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:FOSCARNET SODIUM; 剂型/给药途径:SOLUTION;INTRAVENOUS; 规格:6GM/250ML (24MG/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 |
| 020068 |
001 |
NDA |
FOSCAVIR |
FOSCARNET SODIUM |
SOLUTION;INTRAVENOUS |
6GM/250ML (24MG/ML) |
Prescription |
Yes |
Yes |
AP |
1991/09/27
|
CLINIGEN HLTHCARE |
| 212483 |
001 |
ANDA |
FOSCARNET SODIUM |
FOSCARNET SODIUM |
SOLUTION;INTRAVENOUS |
6GM/250ML (24MG/ML) |
Prescription |
No |
No |
AP |
2021/01/29
|
FRESENIUS KABI USA |
| 213001 |
001 |
ANDA |
FOSCARNET SODIUM |
FOSCARNET SODIUM |
SOLUTION;INTRAVENOUS |
6GM/250ML (24MG/ML) |
Prescription |
No |
No |
AP |
2021/04/21
|
GLAND |
| 213807 |
001 |
ANDA |
FOSCARNET SODIUM |
FOSCARNET SODIUM |
SOLUTION;INTRAVENOUS |
6GM/250ML (24MG/ML) |
Prescription |
No |
No |
AP |
2023/06/05
|
AVET LIFESCIENCES |
| 213987 |
001 |
ANDA |
FOSCARNET SODIUM |
FOSCARNET SODIUM |
SOLUTION;INTRAVENOUS |
6GM/250ML (24MG/ML) |
Prescription |
No |
No |
AP |
2023/11/29
|
SCIECURE |
| 216602 |
001 |
ANDA |
FOSCARNET SODIUM |
FOSCARNET SODIUM |
SOLUTION;INTRAVENOUS |
6GM/250ML (24MG/ML) |
Prescription |
No |
No |
AP |
2024/03/01
|
AMNEAL |