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 |
| 1965/06/23 |
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 |
| 2006/03/29 |
SUPPL-37(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2005/03/17 |
SUPPL-44(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2004/04/16 |
SUPPL-40(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 2001/08/23 |
SUPPL-36(补充) |
Approval |
Labeling |
STANDARD
|
|
|
| 1998/02/13 |
SUPPL-35(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 1989/01/13 |
SUPPL-34(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1988/05/31 |
SUPPL-33(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1987/01/14 |
SUPPL-31(补充) |
Approval |
Labeling |
|
|
|
| 1987/01/14 |
SUPPL-30(补充) |
Approval |
Labeling |
|
|
|
| 1986/07/24 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1986/06/18 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1985/09/17 |
SUPPL-25(补充) |
Approval |
Labeling |
|
|
|
| 1984/05/16 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1983/03/02 |
SUPPL-26(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1982/08/06 |
SUPPL-23(补充) |
Approval |
Labeling |
|
|
|
| 1982/08/06 |
SUPPL-22(补充) |
Approval |
Unspecified |
STANDARD
|
|
|
| 1982/08/06 |
SUPPL-21(补充) |
Approval |
Labeling |
|
|
|
| 1982/08/06 |
SUPPL-20(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1982/03/04 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 1981/09/24 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1980/02/15 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1979/09/11 |
SUPPL-9(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1979/02/15 |
SUPPL-15(补充) |
Approval |
Labeling |
|
|
|
| 1979/02/15 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 1978/11/30 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1978/11/27 |
SUPPL-16(补充) |
Approval |
Labeling |
|
|
|
| 1977/06/20 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 1977/04/06 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1976/11/01 |
SUPPL-8(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1976/05/03 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1976/04/05 |
SUPPL-7(补充) |
Approval |
Labeling |
|
|
|
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:DOXAPRAM HYDROCHLORIDE; 剂型/给药途径:INJECTABLE;INJECTION; 规格:20MG/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 |
| 014879 |
001 |
NDA |
DOPRAM |
DOXAPRAM HYDROCHLORIDE |
INJECTABLE;INJECTION |
20MG/ML |
Prescription |
Yes |
Yes |
AP |
Approved Prior to Jan 1, 1982
|
HIKMA |
| 076266 |
001 |
ANDA |
DOXAPRAM HYDROCHLORIDE |
DOXAPRAM HYDROCHLORIDE |
INJECTABLE;INJECTION |
20MG/ML |
Prescription |
No |
No |
AP |
2003/01/10
|
CHARTWELL INJECTABLE |