药品注册申请号:009112
申请类型:NDA (新药申请)
申请人:JOURNEY
申请人全名:JOURNEY MEDICAL CORP
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
003 EURAX CROTAMITON LOTION;TOPICAL 10% Yes Yes AT 1955/04/29 Approved Prior to Jan 1, 1982 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
2014/10/08 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
2009/07/10 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
2003/06/26 SUPPL-21(补充) Approval Labeling STANDARD
2002/05/23 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1989/04/24 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1987/06/05 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1987/03/03 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1984/11/26 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1984/06/12 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1984/04/25 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1983/09/09 SUPPL-5(补充) Approval Labeling
1983/08/09 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1983/05/09 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1983/03/15 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1983/02/04 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1982/06/30 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1982/06/30 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1981/06/30 SUPPL-7(补充) Approval Labeling
1955/04/29 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:CROTAMITON 剂型/给药途径:LOTION;TOPICAL 规格:10% 治疗等效代码:AT
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
009112 003 NDA EURAX CROTAMITON LOTION;TOPICAL 10% Prescription Yes Yes AT Approved Prior to Jan 1, 1982 JOURNEY
087204 001 ANDA CROTAN CROTAMITON LOTION;TOPICAL 10% Prescription No No AT Approved Prior to Jan 1, 1982 LEGACY PHARMA
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药品NDC数据与药品包装、标签说明书
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