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 |
2018/06/06 |
SUPPL-50(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2017/05/04 |
SUPPL-47(补充) |
Approval |
Labeling |
STANDARD
|
|
|
2002/04/12 |
SUPPL-41(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2001/12/04 |
SUPPL-39(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2001/09/28 |
SUPPL-38(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2001/07/24 |
SUPPL-37(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2001/04/12 |
SUPPL-36(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
2000/10/02 |
SUPPL-35(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1998/05/19 |
SUPPL-34(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1997/09/30 |
SUPPL-33(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1996/12/05 |
SUPPL-32(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1995/08/03 |
SUPPL-30(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1995/05/10 |
SUPPL-31(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1989/10/30 |
SUPPL-29(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1989/10/12 |
SUPPL-28(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1988/09/09 |
SUPPL-27(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1988/02/17 |
SUPPL-26(补充) |
Approval |
Labeling |
|
|
|
1987/11/03 |
SUPPL-25(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1987/04/30 |
SUPPL-24(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1986/06/13 |
SUPPL-23(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1986/06/13 |
SUPPL-22(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1986/04/15 |
SUPPL-21(补充) |
Approval |
Labeling |
|
|
|
1983/07/11 |
SUPPL-16(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/09/03 |
SUPPL-14(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/09/02 |
SUPPL-13(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1982/08/13 |
SUPPL-17(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1980/01/22 |
SUPPL-12(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1979/11/19 |
SUPPL-11(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1975/08/05 |
SUPPL-3(补充) |
Approval |
Labeling |
|
|
|
1974/11/26 |
SUPPL-1(补充) |
Approval |
Manufacturing (CMC) |
STANDARD
|
|
|
1973/05/30 |
ORIG-1(原始申请) |
Approval |
Type 5 - New Formulation or New Manufacturer |
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:PREDNISOLONE ACETATE 剂型/给药途径:SUSPENSION/DROPS;OPHTHALMIC 规格:1% 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 |
017011 |
001 |
NDA |
PRED FORTE |
PREDNISOLONE ACETATE |
SUSPENSION/DROPS;OPHTHALMIC |
1% |
Prescription |
Yes |
Yes |
AB |
Approved Prior to Jan 1, 1982
|
ABBVIE |
017469 |
001 |
NDA |
OMNIPRED |
PREDNISOLONE ACETATE |
SUSPENSION/DROPS;OPHTHALMIC |
1% |
Prescription |
Yes |
Yes |
AB |
Approved Prior to Jan 1, 1982
|
SANDOZ |
216935 |
001 |
ANDA |
PREDNISOLONE ACETATE |
PREDNISOLONE ACETATE |
SUSPENSION/DROPS;OPHTHALMIC |
1% |
Prescription |
No |
No |
AB |
2024/08/02
|
LUPIN LTD |