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 |
| 1965/10/18 |
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 |
| 2013/07/23 |
SUPPL-37(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2013/06/12 |
SUPPL-36(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2012/12/14 |
SUPPL-35(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 2008/03/25 |
SUPPL-32(补充) |
Approval |
Labeling-Container/Carton Labels |
N/A
|
|
|
| 2002/07/17 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 1998/11/06 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 1991/08/30 |
SUPPL-26(补充) |
Approval |
Manufacturing (CMC)-Packaging |
STANDARD
|
|
|
| 1990/10/02 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC)-Packaging |
STANDARD
|
|
|
| 1987/12/18 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1987/06/03 |
SUPPL-23(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
| 1986/11/14 |
SUPPL-22(补充) |
Approval |
Labeling |
|
|
|
| 1982/10/08 |
SUPPL-21(补充) |
Approval |
Labeling |
|
|
|
| 1980/08/12 |
SUPPL-20(补充) |
Approval |
Labeling |
|
|
|
| 1979/11/26 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1978/07/24 |
SUPPL-16(补充) |
Approval |
Labeling |
|
|
|
| 1978/06/30 |
SUPPL-17(补充) |
Approval |
Labeling |
|
|
|
| 1977/12/14 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC)-Expiration Date |
STANDARD
|
|
|
| 1977/11/11 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
| 1977/02/23 |
SUPPL-14(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:FLURANDRENOLIDE; 剂型/给药途径:OINTMENT;TOPICAL; 规格:0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; 治疗等效代码:AT<<<
| 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 |
| 012806 |
001 |
NDA |
CORDRAN |
FLURANDRENOLIDE |
OINTMENT;TOPICAL |
0.05% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
Discontinued |
Yes |
No |
AT |
Approved Prior to Jan 1, 1982
|
INA PHARMS |