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 |
2016/07/29 |
SUPPL-16(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2016/04/11 |
SUPPL-15(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2013/05/15 |
SUPPL-12(补充) |
Approval |
Labeling |
STANDARD
;Orphan
|
|
|
2013/03/22 |
SUPPL-11(补充) |
Approval |
Efficacy |
PRIORITY
|
|
|
2012/11/27 |
SUPPL-10(补充) |
Approval |
Manufacturing (CMC) |
PRIORITY
|
|
|
2012/06/13 |
SUPPL-3(补充) |
Approval |
Efficacy |
STANDARD
;Orphan
|
|
|
2009/03/20 |
SUPPL-1(补充) |
Approval |
Labeling |
STANDARD
;Orphan
|
|
|
2008/06/23 |
ORIG-1(原始申请) |
Approval |
Type 1 - New Molecular Entity |
PRIORITY
;Orphan
|
|
|
与本品治疗等效的药品
活性成分:DIFLUPREDNATE 剂型/给药途径:EMULSION;OPHTHALMIC 规格:0.05% 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 |
219441 |
001 |
ANDA |
DIFLUPREDNATE |
DIFLUPREDNATE |
EMULSION;OPHTHALMIC |
0.05% |
Prescription |
No |
No |
AB |
--
|
CAPLIN |
022212 |
001 |
NDA |
DUREZOL |
DIFLUPREDNATE |
EMULSION;OPHTHALMIC |
0.05% |
Prescription |
Yes |
Yes |
AB |
2008/06/23
|
SANDOZ |
211776 |
001 |
ANDA |
DIFLUPREDNATE |
DIFLUPREDNATE |
EMULSION;OPHTHALMIC |
0.05% |
Prescription |
No |
No |
AB |
2021/08/09
|
CIPLA |
211526 |
001 |
ANDA |
DIFLUPREDNATE |
DIFLUPREDNATE |
EMULSION;OPHTHALMIC |
0.05% |
Prescription |
No |
No |
AB |
2021/11/17
|
AMNEAL |
214894 |
001 |
ANDA |
DIFLUPREDNATE |
DIFLUPREDNATE |
EMULSION;OPHTHALMIC |
0.05% |
Prescription |
No |
No |
AB |
2022/11/16
|
DR REDDYS |
207284 |
001 |
ANDA |
DIFLUPREDNATE |
DIFLUPREDNATE |
EMULSION;OPHTHALMIC |
0.05% |
Prescription |
No |
No |
AB |
2024/05/14
|
EPIC PHARMA LLC |