cephalexin头孢氨苄_FDA数据库

药智数据企业版注册数据库：增设了"联合申报"、"临床试验默认许可日期"等搜索条件，让搜索页面纬度更加全面，还有热点搜索和高级条件组合检索等检索功能等你来体验！

申请号

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参比制剂

商品名

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标准制剂

活性成分

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有无专利

活性成分

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批准时间

申请机构

专利到期日

剂型/给药途径

物质专利到期日

规格/剂量

产品专利到期日

申请类型

专营保护到期日

市场状态

专利号查询

1. 列表页商品名字段中有红色标记P代表该数据有专利信息；当使用各个专利到期时间检索条件时，“有无专利”默认为有。

2. 批准日期显示1982-01-01的，实际为1982-01-01之前。

3. 更多参比制剂一次性进口信息

你目前无法使用部分二次筛选功能请联系客服开通更多权限和功能！

导出数据

申请号	产品号	商品名	活性成分	活性成分	剂型/给药途径	规格/剂量	申请机构	批准时间	参比制剂	标准制剂	市场状态
(NDA) 050406	001	KEFLEX	CEPHALEXIN	头孢氨苄	FOR SUSPENSION;ORAL	EQ 125MG BASE/5ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAGMA	1982-01-01	Yes	No	DISCN
(NDA) 050406	002	KEFLEX	CEPHALEXIN	头孢氨苄	FOR SUSPENSION;ORAL	EQ 250MG BASE/5ML *Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAGMA	1982-01-01	Yes	No	DISCN
(NDA) 050406	003	KEFLEX	CEPHALEXIN	头孢氨苄	FOR SUSPENSION;ORAL	EQ 100MG BASE/ML *Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAGMA	1982-01-01	Yes	No	DISCN
(NDA) 050405	002	KEFLEX	CEPHALEXIN	头孢氨苄	CAPSULE;ORAL	EQ 250MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAGMA	1982-01-01	Yes	No	DISCN
(NDA) 050405	003	KEFLEX	CEPHALEXIN	头孢氨苄	CAPSULE;ORAL	EQ 500MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAGMA	1982-01-01	Yes	No	DISCN
(NDA) 050405	004	KEFLEX	CEPHALEXIN	头孢氨苄	CAPSULE;ORAL	EQ 333MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAGMA	2006-05-12	Yes	No	DISCN
(NDA) 050405	005	KEFLEX	CEPHALEXIN	头孢氨苄	CAPSULE;ORAL	EQ 750MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	PRAGMA	2006-05-12	Yes	No	DISCN