药品注册申请号:075292
申请类型:ANDA (仿制药申请)
申请人:NOSTRUM LABS INC
申请人全名:NOSTRUM LABORATORIES INC
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 FLUOXETINE HYDROCHLORIDE FLUOXETINE HYDROCHLORIDE SOLUTION;ORAL EQ 20MG BASE/5ML No No AA 2002/02/07 2002/02/07 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
2023/08/18 SUPPL-24(补充) Approval Labeling STANDARD
2023/08/09 SUPPL-23(补充) Approval Labeling STANDARD
2021/09/20 SUPPL-21(补充) Approval Labeling STANDARD
2021/09/12 SUPPL-20(补充) Approval Labeling STANDARD
2017/01/04 SUPPL-19(补充) Approval Labeling STANDARD
2014/09/02 SUPPL-18(补充) Approval Labeling STANDARD
2012/05/29 SUPPL-17(补充) Approval Labeling
2008/12/02 SUPPL-15(补充) Approval Labeling
2007/06/29 SUPPL-12(补充) Approval Labeling
2007/06/29 SUPPL-11(补充) Approval Labeling
2006/08/29 SUPPL-10(补充) Approval Labeling
2006/08/29 SUPPL-9(补充) Approval Labeling
2006/03/15 SUPPL-7(补充) Approval Labeling
2005/05/17 SUPPL-5(补充) Approval Labeling
2005/05/17 SUPPL-4(补充) Approval Labeling
2002/09/03 SUPPL-1(补充) Approval Manufacturing (CMC)
2002/02/07 ORIG-1(原始申请) Approval
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:FLUOXETINE HYDROCHLORIDE 剂型/给药途径:SOLUTION;ORAL 规格:EQ 20MG 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
075506 001 ANDA FLUOXETINE HYDROCHLORIDE FLUOXETINE HYDROCHLORIDE SOLUTION;ORAL EQ 20MG BASE/5ML Prescription No No AA 2001/08/02 TEVA
076015 001 ANDA FLUOXETINE HYDROCHLORIDE FLUOXETINE HYDROCHLORIDE SOLUTION;ORAL EQ 20MG BASE/5ML Prescription No Yes AA 2002/01/30 PHARM ASSOC
075292 001 ANDA FLUOXETINE HYDROCHLORIDE FLUOXETINE HYDROCHLORIDE SOLUTION;ORAL EQ 20MG BASE/5ML Prescription No No AA 2002/02/07 NOSTRUM LABS INC
075514 001 ANDA FLUOXETINE HYDROCHLORIDE FLUOXETINE HYDROCHLORIDE SOLUTION;ORAL EQ 20MG BASE/5ML Discontinued No No AA 2002/08/29 PHARMOBEDIENT CNSLTG
077849 001 ANDA FLUOXETINE HYDROCHLORIDE FLUOXETINE HYDROCHLORIDE SOLUTION;ORAL EQ 20MG BASE/5ML Prescription No No AA 2007/02/09 LANNETT CO INC
079209 001 ANDA FLUOXETINE HYDROCHLORIDE FLUOXETINE HYDROCHLORIDE SOLUTION;ORAL EQ 20MG BASE/5ML Prescription No No AA 2009/03/20 AUROBINDO PHARMA
216448 001 ANDA FLUOXETINE HYDROCHLORIDE FLUOXETINE HYDROCHLORIDE SOLUTION;ORAL EQ 20MG BASE/5ML Prescription No No AA 2022/11/09 NOVITIUM PHARMA
216953 001 ANDA FLUOXETINE HYDROCHLORIDE FLUOXETINE HYDROCHLORIDE SOLUTION;ORAL EQ 20MG BASE/5ML Prescription No No AA 2022/11/15 APTAPHARMA INC
更多信息
药品NDC数据与药品包装、标签说明书
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