药品注册申请号:017433
申请类型:NDA (新药申请)
申请人:DAVIS AND GECK
申请人全名:DAVIS AND GECK DIV AMERICAN CYANAMID CO
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 PRE-OP HEXACHLOROPHENE SPONGE;TOPICAL 480MG Yes Yes AT 1978/10/12 Approved Prior to Jan 1, 1982 Prescription
002 PRE-OP II HEXACHLOROPHENE SPONGE;TOPICAL 480MG Yes No AT 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
1992/05/07 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1992/04/01 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1989/11/28 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1985/08/30 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1985/07/23 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1985/03/25 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1985/02/05 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1983/03/28 SUPPL-9(补充) Approval Manufacturing (CMC) STANDARD
1983/03/28 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1982/11/29 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1982/06/30 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1980/12/01 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1980/12/01 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1980/08/26 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1980/02/11 SUPPL-2(补充) Approval Labeling
1978/10/12 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
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:HEXACHLOROPHENE 剂型/给药途径:SPONGE;TOPICAL 规格:480MG 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
017433 001 NDA PRE-OP HEXACHLOROPHENE SPONGE;TOPICAL 480MG Prescription Yes Yes AT Approved Prior to Jan 1, 1982 DAVIS AND GECK
017433 002 NDA PRE-OP II HEXACHLOROPHENE SPONGE;TOPICAL 480MG Prescription Yes No AT Approved Prior to Jan 1, 1982 DAVIS AND GECK
活性成分:HEXACHLOROPHENE 剂型/给药途径:SPONGE;TOPICAL 规格:480MG 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
017433 001 NDA PRE-OP HEXACHLOROPHENE SPONGE;TOPICAL 480MG Prescription Yes Yes AT Approved Prior to Jan 1, 1982 DAVIS AND GECK
017433 002 NDA PRE-OP II HEXACHLOROPHENE SPONGE;TOPICAL 480MG Prescription Yes No AT Approved Prior to Jan 1, 1982 DAVIS AND GECK
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