药品名称BREVITAL SODIUM
申请号011559产品号004
活性成分METHOHEXITAL SODIUM市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格200MG/VIAL
治疗等效代码参比药物
批准日期2012/12/21申请机构PAR STERILE PRODUCTS LLC
化学类型New molecular entity (NME)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
011559045APLetter2014/01/24下载
011559045APLabel2014/01/28下载
011559041APLetter2008/05/08下载
011559041APLabel2008/06/12下载
011559037APLabel2004/06/01下载
011559037APLetter2004/06/01下载
011559033APLetter2004/05/28下载
011559032APLetter2001/07/13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
011559048AP2014/12/15Manufacturing Change or Addition
011559047AP2014/09/22Manufacturing Change or Addition
011559045AP2014/01/23Labeling Revision
011559041AP2008/05/05Labeling Revision
011559037AP2004/05/27Labeling Revision
011559033AP2003/03/14Manufacturing Change or Addition
011559032AP2001/07/13Labeling Revision
011559030AP1997/12/17Labeling Revision
011559029AP1998/01/30New Route of Administration
011559028AP1998/01/30New Route of Administration
011559027AP1996/07/25Control Supplement
011559026AP1996/02/29Manufacturing Change or Addition
011559025AP1995/11/02Package Change
011559024AP1994/06/14Control Supplement
011559021AP1992/12/02Labeling Revision
011559018AP1992/12/18Labeling Revision
011559014AP1988/07/08Labeling Revision
011559012AP1981/07/01Control Supplement
011559010AP1979/10/04Control Supplement
011559009AP1976/05/14Labeling Revision
011559008AP1975/06/13Labeling Revision
011559004AP1969/12/11Labeling Revision
011559000AP1960/06/27Approval