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 |
1960/01/04 |
ORIG-1(原始申请) |
Approval |
Type 3 - New Dosage Form |
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 |
2024/08/14 |
SUPPL-52(补充) |
Approval |
Manufacturing (CMC)-Packaging |
N/A
|
|
|
2024/06/05 |
SUPPL-51(补充) |
Approval |
Labeling-Container/Carton Labels |
STANDARD
|
|
|
2018/06/22 |
SUPPL-45(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
2018/03/29 |
SUPPL-44(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
2015/10/26 |
SUPPL-43(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2014/07/03 |
SUPPL-42(补充) |
Approval |
Labeling-Package Insert |
STANDARD
|
|
|
2011/07/15 |
SUPPL-39(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2011/06/16 |
SUPPL-38(补充) |
Approval |
Labeling |
UNKNOWN
|
|
|
2010/01/28 |
SUPPL-36(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2006/11/20 |
SUPPL-33(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2001/06/15 |
SUPPL-34(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1998/02/03 |
SUPPL-32(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
1996/05/22 |
SUPPL-31(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
1995/01/10 |
SUPPL-30(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
1993/10/06 |
SUPPL-27(补充) |
Approval |
Labeling |
|
|
|
1993/08/30 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC)-Packaging |
STANDARD
|
|
|
1993/08/30 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC)-Packaging |
STANDARD
|
|
|
1991/09/25 |
SUPPL-26(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
1991/07/19 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC)-Packaging |
STANDARD
|
|
|
1987/11/30 |
SUPPL-23(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1986/11/19 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1985/12/03 |
SUPPL-22(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/01/12 |
SUPPL-14(补充) |
Approval |
Labeling |
|
|
|
1981/04/01 |
SUPPL-21(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
1980/05/20 |
SUPPL-18(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
1979/08/21 |
SUPPL-19(补充) |
Approval |
Manufacturing (CMC)-Control |
STANDARD
|
|
|
1979/07/17 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1978/12/28 |
SUPPL-13(补充) |
Approval |
Labeling |
|
|
|
1977/09/19 |
SUPPL-16(补充) |
Approval |
Manufacturing (CMC)-Control |
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:TRIAMCINOLONE ACETONIDE; 剂型/给药途径:INJECTABLE;INJECTION; 规格:10MG/ML; 治疗等效代码:AB<<<
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 |
012041 |
001 |
NDA |
KENALOG-10 |
TRIAMCINOLONE ACETONIDE |
INJECTABLE;INJECTION |
10MG/ML |
Prescription |
Yes |
No |
AB |
Approved Prior to Jan 1, 1982
|
APOTHECON |
218773 |
001 |
ANDA |
TRIAMCINOLONE ACETONIDE |
TRIAMCINOLONE ACETONIDE |
INJECTABLE;INJECTION |
10MG/ML |
Prescription |
No |
No |
AB |
2025/03/12
|
DR REDDYS |