药品注册申请号:019157
申请类型:NDA (新药申请)
申请人:SETON PHARM
申请人全名:SETON PHARMACEUTICAL LLC
产品信息
产品号商品名活性成分剂型/给药途径规格/剂量参比药物(RLD)生物等效参考标准(RS)治疗等效代码该申请号批准日期该产品号批准日期市场状态
001 PEDIAPRED PREDNISOLONE SODIUM PHOSPHATE SOLUTION;ORAL EQ 5MG BASE/5ML Yes Yes AA 1986/05/28 1986/05/28 Prescription
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
2024/06/05 SUPPL-25(补充) Approval Labeling STANDARD
2018/02/05 SUPPL-21(补充) Approval Labeling STANDARD
2013/10/08 SUPPL-20(补充) Approval Labeling STANDARD
2004/12/03 SUPPL-18(补充) Approval Labeling STANDARD
2002/01/03 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1998/12/17 SUPPL-15(补充) Approval Efficacy STANDARD
1998/12/17 SUPPL-13(补充) Approval Labeling STANDARD
1998/12/17 SUPPL-12(补充) Approval Labeling STANDARD
1998/12/17 SUPPL-11(补充) Approval Labeling STANDARD
1998/01/21 SUPPL-16(补充) Approval Labeling STANDARD
1997/05/29 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1995/05/10 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1993/11/22 SUPPL-9(补充) Approval Labeling STANDARD
1993/11/08 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1989/10/27 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1989/02/02 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1988/10/31 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1986/08/14 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1986/05/28 ORIG-1(原始申请) Approval Type 3 - New Dosage Form 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
与本品相关的市场独占权保护信息
关联产品号独占权代码失效日期备注
与本品治疗等效的药品
活性成分:PREDNISOLONE SODIUM PHOSPHATE 剂型/给药途径:SOLUTION;ORAL 规格:EQ 5MG BASE/5ML 治疗等效代码:AA
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RLDRSTE Code产品号批准日期申请人
019157 001 NDA PEDIAPRED PREDNISOLONE SODIUM PHOSPHATE SOLUTION;ORAL EQ 5MG BASE/5ML Prescription Yes Yes AA 1986/05/28 SETON PHARM
075099 001 ANDA PREDNISOLONE SODIUM PHOSPHATE PREDNISOLONE SODIUM PHOSPHATE SOLUTION;ORAL EQ 5MG BASE/5ML Discontinued No No AA 2002/06/28 PHARMOBEDIENT CNSLTG
075183 001 ANDA PREDNISOLONE SODIUM PHOSPHATE PREDNISOLONE SODIUM PHOSPHATE SOLUTION;ORAL EQ 5MG BASE/5ML Discontinued No No AA 2003/03/26 HIKMA
075988 001 ANDA PREDNISOLONE SODIUM PHOSPHATE PREDNISOLONE SODIUM PHOSPHATE SOLUTION;ORAL EQ 5MG BASE/5ML Prescription No No AA 2004/05/25 CHARTWELL RX
更多信息
药品NDC数据与药品包装、标签说明书
©2006-2024 DrugFuture->U.S. FDA Drugs Database