药品注册申请号:019599
申请类型:NDA (新药申请)
申请人:LEGACY PHARMA
申请人全名:LEGACY PHARMA 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 NAFTIN NAFTIFINE HYDROCHLORIDE CREAM;TOPICAL 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None 1988/02/29 1988/02/29 Discontinued
002 NAFTIN NAFTIFINE HYDROCHLORIDE CREAM;TOPICAL 2% Yes Yes AB 2012/01/13 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
2018/04/30 SUPPL-14(补充) Approval Labeling STANDARD
2016/11/10 SUPPL-13(补充) Approval Efficacy STANDARD
2014/10/10 SUPPL-12(补充) Approval Efficacy STANDARD
2012/01/13 SUPPL-11(补充) Approval Efficacy STANDARD
2009/01/26 SUPPL-10(补充) Approval Manufacturing (CMC) N/A
2006/08/10 SUPPL-9(补充) Approval Manufacturing (CMC) N/A
2002/06/04 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1998/11/30 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1997/09/24 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1995/06/15 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1990/07/05 SUPPL-2(补充) Approval Efficacy
1990/01/30 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1989/04/05 SUPPL-1(补充) Approval Efficacy
1988/02/29 ORIG-1(原始申请) Approval Type 1 - New Molecular Entity 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
002 M-191 2019/11/10**本条是由Drugfuture回溯的历史信息**
NS 2015/01/13**本条是由Drugfuture回溯的历史信息**
与本品治疗等效的药品
活性成分:NAFTIFINE HYDROCHLORIDE 剂型/给药途径:CREAM;TOPICAL 规格:2% 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RLDRSTE Code产品号批准日期申请人
019599 002 NDA NAFTIN NAFTIFINE HYDROCHLORIDE CREAM;TOPICAL 2% Prescription Yes Yes AB 2012/01/13 LEGACY PHARMA
206901 001 ANDA NAFTIFINE HYDROCHLORIDE NAFTIFINE HYDROCHLORIDE CREAM;TOPICAL 2% Prescription No No AB 2016/01/06 TARO
206960 001 ANDA NAFTIFINE HYDROCHLORIDE NAFTIFINE HYDROCHLORIDE CREAM;TOPICAL 2% Prescription No No AB 2017/04/10 AMNEAL
210038 001 ANDA NAFTIFINE HYDROCHLORIDE NAFTIFINE HYDROCHLORIDE CREAM;TOPICAL 2% Prescription No No AB 2020/09/22 XIROMED
更多信息
药品NDC数据与药品包装、标签说明书
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