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 |
2023/12/15 |
SUPPL-29(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2022/08/08 |
SUPPL-24(补充) |
Tentative Approval |
Manufacturing (CMC) |
N/A
|
|
|
2019/10/07 |
SUPPL-23(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/12/16 |
SUPPL-21(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2015/07/24 |
SUPPL-19(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1999/05/25 |
SUPPL-16(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1998/01/20 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1997/01/28 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1995/10/30 |
SUPPL-13(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1995/08/03 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1995/02/22 |
SUPPL-11(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1994/08/18 |
SUPPL-9(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1994/01/07 |
SUPPL-6(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1994/01/07 |
SUPPL-5(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1993/11/22 |
SUPPL-8(补充) |
Approval |
Efficacy |
STANDARD
|
|
|
1992/11/10 |
SUPPL-7(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1991/08/07 |
SUPPL-4(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1990/12/06 |
SUPPL-3(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1990/07/05 |
SUPPL-2(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1988/07/28 |
SUPPL-1(补充) |
Approval |
Labeling |
|
|
|
1986/12/29 |
ORIG-1(原始申请) |
Approval |
Type 1 - New Molecular Entity |
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 |
无 |
与本品治疗等效的药品
活性成分:ALFENTANIL HYDROCHLORIDE 剂型/给药途径:INJECTABLE;INJECTION 规格:EQ 0.5MG BASE/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 |
019353 |
001 |
NDA |
ALFENTA |
ALFENTANIL HYDROCHLORIDE |
INJECTABLE;INJECTION |
EQ 0.5MG BASE/ML |
Prescription |
Yes |
Yes |
AP |
1986/12/29
|
RISING |
075221 |
001 |
ANDA |
ALFENTANIL |
ALFENTANIL HYDROCHLORIDE |
INJECTABLE;INJECTION |
EQ 0.5MG BASE/ML |
Prescription |
No |
No |
AP |
1999/10/28
|
HOSPIRA |