药品名称DIURIL
申请号011145产品号005
活性成分CHLOROTHIAZIDE SODIUM市场状态处方药
剂型或给药途径INJECTABLE;INJECTION规格EQ 500MG BASE/VIAL
治疗等效代码AP参比药物
批准日期Approved Prior to Jan 1, 1982申请机构OAK PHARMACEUTICALS INC SUB AKORN INC
化学类型New molecular entity (NME)审评分类Priority 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
011145093APLetter2005/08/11下载
011145092APLetter2004/10/29下载
011145091APLetter2004/09/29下载
011145090APLetter2004/09/29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
011145098AP2013/03/20Manufacturing Change or Addition
011145093AP2005/08/10Labeling Revision
011145092AP2004/10/22Labeling Revision
011145091AP2004/09/23Labeling Revision
011145090AP2004/09/23Labeling Revision
011145089AP2002/11/08Manufacturing Change or Addition
011145088AP1999/09/08Formulation Revision
011145087AP1997/09/05Control Supplement
011145086AP1997/05/05Manufacturing Change or Addition
011145085AP1998/12/09Labeling Revision
011145084AP1995/11/29Manufacturing Change or Addition
011145083AP1995/05/23Labeling Revision
011145082AP1995/05/23Labeling Revision
011145081AP1994/03/16Manufacturing Change or Addition
011145080AP1994/03/31Labeling Revision
011145079AP1993/03/02Labeling Revision
011145078AP1994/02/16Labeling Revision
011145075AP1989/05/30Manufacturing Change or Addition
011145074AP1993/03/02Labeling Revision
011145073AP1993/03/02Labeling Revision
011145068AP1986/12/08Manufacturing Change or Addition
011145064AP1986/01/14Labeling Revision
011145063AP1986/01/13Labeling Revision
011145062AP1985/11/04Labeling Revision
011145061AP1984/10/11Package Change
011145060AP1985/08/27Package Change
011145059AP1984/10/11Package Change
011145058AP1984/09/24Labeling Revision
011145057AP1984/08/28Labeling Revision
011145056AP1984/08/30Package Change
011145055AP1984/03/06Labeling Revision
011145054AP1984/03/06Labeling Revision
011145053AP1983/03/01Package Change
011145052AP1982/04/19Manufacturing Change or Addition
011145051AP1981/07/14Package Change
011145050AP1981/11/03Manufacturing Change or Addition
011145049AP1981/06/17Package Change
011145048AP1987/05/08Practioner Draft Labeling
011145046AP1981/01/13Labeling Revision
011145045AP1981/01/13Labeling Revision
011145044AP1980/11/14Package Change
011145043AP1979/10/31Labeling Revision
011145042AP1979/10/31Labeling Revision
011145041AP1979/07/13Labeling Revision
011145040AP1979/10/31Labeling Revision
011145039AP1979/10/31Labeling Revision
011145038AP1979/03/09Control Supplement
011145037AP1979/10/31Labeling Revision
011145036AP1979/10/31Labeling Revision
011145035AP1978/07/31Labeling Revision
011145034AP1978/02/15Package Change
011145033AP1977/05/02Package Change
011145031AP1979/10/31Labeling Revision
011145027AP1976/01/12Control Supplement
011145026AP1975/12/12Control Supplement
011145020AP1975/03/27Other Amendment
011145019AP1975/03/27Other Amendment
011145000AP1958/09/04Approval