药品名称VANTIN
申请号050675产品号001
活性成分CEFPODOXIME PROXETIL市场状态停止上市
剂型或给药途径FOR SUSPENSION;ORAL规格EQ 50MG BASE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**
治疗等效代码参比药物
批准日期1992/08/07申请机构PHARMACIA AND UPJOHN CO
化学类型New dosage form审评分类Standard review drug
与本品相关的专利信息(来自橙皮书Orange Book)
专利号专利过期日是否化合物专利是否产品专利专利用途代码专利下载
历史专利信息
与本品相关的市场独占权保护信息
独占权代码失效日期
历史市场独占权保护信息
与药品注册相关的信息
申请号修订号审批结论公开文档类型文档创建时间获取文档
050675018APLetter2013/06/24下载
050675018APLabel2013/06/25下载
050675017APLetter2007/06/07下载
050675017APLabel2007/06/07下载
050675016APLetter2004/06/07下载
050675016APLabel2004/06/07下载
050675015APLetter1998/11/20下载
050675015APReview1999/07/27下载
050675014APLetter1998/11/20下载
050675014APReview1998/11/20下载
药品注册审批历史信息
申请号修订号审批结论审批日期审批内容
050675018AP2013/06/21Labeling Revision
050675017AP2007/06/05Labeling Revision
050675016AP2004/06/02Labeling Revision
050675015AP1998/11/20New or Modified Indication
050675014AP1998/11/20New Dosage Regimen
050675013AP1997/03/19Labeling Revision
050675012AP1996/12/09Control Supplement
050675011AP1995/09/28Labeling Revision
050675010AP1996/03/14Labeling Revision
050675009AP1996/03/14New or Modified Indication
050675008AP1996/05/07New Dosage Regimen
050675007AP1994/07/06Labeling Revision
050675006AP1993/11/02Labeling Revision
050675005AP1993/10/20Labeling Revision
050675004AP1993/04/22Labeling Revision
050675003AP1995/06/16Comparative Efficacy Claim
050675002AP1993/04/08Labeling Revision
050675001AP1993/10/12Labeling Revision
050675000AP1992/08/07Approval