药品注册申请号:020325
申请类型:NDA (新药申请)
申请人:KENVUE BRANDS
申请人全名:KENVUE BRANDS LLC
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 PEPCID AC FAMOTIDINE TABLET;ORAL 10MG Yes No None 1995/04/28 1995/04/28 Over-the-counter
002 PEPCID AC FAMOTIDINE TABLET;ORAL 20MG Yes Yes None 2003/09/23 Over-the-counter
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
>>>原始批准或临时批准<<<
审批日期提交号审批结论提交分类审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
1995/04/28 ORIG-1(原始申请) Approval Type 5 - New Formulation or New Manufacturer STANDARD
>>>补充申请<<<
审批日期提交号审批结论补充类别或审批类型审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
2023/12/14 SUPPL-43(补充) Approval Manufacturing (CMC)-Formulation N/A
2022/12/15 SUPPL-41(补充) Approval Labeling-Container/Carton Labels STANDARD
2022/02/18 SUPPL-37(补充) Approval Labeling-Container/Carton Labels N/A
2019/04/09 SUPPL-33(补充) Approval Labeling-Container/Carton Labels STANDARD
2016/08/01 SUPPL-31(补充) Approval Manufacturing (CMC) STANDARD
2016/06/08 SUPPL-30(补充) Approval Labeling-Container/Carton Labels STANDARD
2016/05/05 SUPPL-29(补充) Approval Manufacturing (CMC) STANDARD
2015/07/09 SUPPL-28(补充) Approval Manufacturing (CMC) STANDARD
2015/05/06 SUPPL-27(补充) Approval Manufacturing (CMC) STANDARD
2015/04/20 SUPPL-26(补充) Approval Manufacturing (CMC) STANDARD
2013/04/01 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
2012/10/11 SUPPL-24(补充) Approval Labeling-Container/Carton Labels STANDARD
2006/06/09 SUPPL-19(补充) Approval Labeling STANDARD
2004/10/27 SUPPL-17(补充) Approval Labeling STANDARD
2003/09/23 SUPPL-15(补充) Approval Efficacy-New Dosing Regimen STANDARD
2002/03/01 SUPPL-13(补充) Approval Labeling STANDARD
2000/04/05 SUPPL-11(补充) Approval Manufacturing (CMC)-Packaging STANDARD
2000/02/10 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1998/11/09 SUPPL-7(补充) Approval Efficacy-New Dosing Regimen STANDARD
1998/11/05 SUPPL-9(补充) Approval Manufacturing (CMC)-Control STANDARD
1998/04/15 SUPPL-8(补充) Approval Manufacturing (CMC)-Packaging STANDARD
1997/09/26 SUPPL-6(补充) Approval Manufacturing (CMC)-Packaging STANDARD
1996/05/31 SUPPL-1(补充) Approval Manufacturing (CMC)-Control STANDARD
1996/05/03 SUPPL-3(补充) Approval Manufacturing (CMC)-Packaging STANDARD
1996/04/23 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1995/10/02 SUPPL-2(补充) Approval Manufacturing (CMC) 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
001 5854267 2015/12/29 U-267 PDF格式**本条是由Drugfuture回溯的历史信息**
5854267*PED 2016/06/29 U-267 PDF格式**本条是由Drugfuture回溯的历史信息**
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 NP 2006/09/23**本条是由Drugfuture回溯的历史信息**
与本品治疗等效的药品
本品无治疗等效药品
更多信息
药品NDC数据与药品包装、标签说明书
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