药品名称OVCON-35
申请号017716产品号001
活性成分ETHINYL ESTRADIOL; NORETHINDRONE市场状态停止上市
剂型或给药途径TABLET;ORAL-28规格0.035MG;0.4MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**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Approved Prior to Jan 1, 1982申请机构WARNER CHILCOTT CO LLC
化学类型New dosage form审评分类Standard review drug
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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
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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
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
017716047AP1998/12/21Manufacturing Change or Addition
017716046AP1997/11/14Control Supplement
017716045AP1998/08/10Labeling Revision
017716044AP1995/07/07Package Change
017716043AP1995/01/25Labeling Revision
017716042AP1993/03/12Control Supplement
017716041AP1994/04/08Manufacturing Change or Addition
017716039AP1993/03/12Labeling Revision
017716038AP1995/02/14Labeling Revision
017716037AP1992/07/21Labeling Revision
017716036AP1991/07/24Manufacturing Change or Addition
017716035AP1991/03/12Control Supplement
017716033AP1989/08/24Labeling Revision
017716032AP1986/03/18Control Supplement
017716029AP1984/09/27Package Change
017716028AP1984/12/03Labeling Revision
017716027AP1984/01/23Control Supplement
017716026AP1983/03/25Labeling Revision
017716025AP1984/02/08Control Supplement
017716024AP1982/11/05Control Supplement
017716022AP1981/04/14Labeling Revision
017716019AP1980/01/14Labeling Revision
017716018AP1979/08/28Package Change
017716017AP1979/06/04Labeling Revision
017716015AP1979/01/19Labeling Revision
017716014AP1978/10/20Expiration Date Change
017716013AP1978/06/08Manufacturing Change or Addition
017716012AP1978/07/14Labeling Revision
017716011AP1978/10/18Control Supplement
017716010AP1978/10/18Control Supplement
017716009AP1978/04/28Labeling Revision
017716008AP1978/07/14Labeling Revision
017716006AP1978/04/28Labeling Revision
017716001AP1976/04/30Labeling Revision
017716000AP1976/03/29Approval