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 |
2001/11/26 |
SUPPL-39(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2000/12/14 |
SUPPL-37(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2000/04/12 |
SUPPL-36(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2000/02/18 |
SUPPL-35(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1998/09/29 |
SUPPL-34(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1995/03/15 |
SUPPL-32(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1995/02/22 |
SUPPL-33(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1994/06/29 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1994/03/02 |
SUPPL-30(补充) |
Approval |
Labeling |
STANDARD
|
|
|
1992/10/28 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1990/10/05 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1988/12/06 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1987/12/31 |
SUPPL-20(补充) |
Approval |
Labeling |
|
|
|
1987/12/31 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1987/07/17 |
SUPPL-26(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1987/04/02 |
SUPPL-22(补充) |
Approval |
Labeling |
|
|
|
1986/12/15 |
SUPPL-24(补充) |
Approval |
Labeling |
|
|
|
1986/12/15 |
SUPPL-23(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1985/03/15 |
SUPPL-21(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/08/13 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/07/28 |
SUPPL-13(补充) |
Approval |
Labeling |
|
|
|
1982/07/28 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/01/20 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1980/05/23 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1976/11/08 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1974/08/29 |
SUPPL-5(补充) |
Approval |
Labeling |
|
|
|
1970/06/11 |
ORIG-1(原始申请) |
Approval |
Type 3 - New Dosage Form |
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:DROPERIDOL 剂型/给药途径:INJECTABLE;INJECTION 规格:2.5MG/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 |
016796 |
001 |
NDA |
INAPSINE |
DROPERIDOL |
INJECTABLE;INJECTION |
2.5MG/ML |
Discontinued |
Yes |
No |
AP |
Approved Prior to Jan 1, 1982
|
RISING |
071981 |
001 |
ANDA |
DROPERIDOL |
DROPERIDOL |
INJECTABLE;INJECTION |
2.5MG/ML |
Discontinued |
No |
No |
AP |
1988/02/29
|
HOSPIRA |
072123 |
001 |
ANDA |
DROPERIDOL |
DROPERIDOL |
INJECTABLE;INJECTION |
2.5MG/ML |
Prescription |
No |
Yes |
AP |
1988/10/24
|
AM REGENT |
208197 |
001 |
ANDA |
DROPERIDOL |
DROPERIDOL |
INJECTABLE;INJECTION |
2.5MG/ML |
Discontinued |
No |
No |
AP |
2017/12/14
|
HIKMA |