药品名称NORINYL 1+80 28-DAY
申请号016725产品号001
活性成分MESTRANOL; NORETHINDRONE市场状态停止上市
剂型或给药途径TABLET;ORAL-28规格0.08MG;1MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构GD SEARLE LLC
化学类型New formulation or new manufacturer审评分类Standard review drug
与本品相关的专利信息(来自橙皮书Orange Book)
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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
016725108AP1986/07/11Labeling Revision
016725107AP1985/10/25Labeling Revision
016725106AP1985/04/16Labeling Revision
016725104AP1984/11/13Manufacturing Change or Addition
016725103AP1984/09/27Control Supplement
016725102AP1984/07/30Labeling Revision
016725101AP1984/06/12Labeling Revision
016725099AP1984/05/07Labeling Revision
016725098AP1983/07/26Control Supplement
016725097AP1983/07/19Control Supplement
016725096AP1983/07/19Control Supplement
016725095AP1984/03/06Labeling Revision
016725094AP1983/07/26Control Supplement
016725093AP1983/06/13Control Supplement
016725089AP1982/07/29Control Supplement
016725085AP1982/01/11Control Supplement
016725079AP1980/04/20Formulation Revision
016725078AP1979/07/18Manufacturing Change or Addition
016725075AP1979/07/18Control Supplement
016725070AP1978/11/06Control Supplement
016725069AP1978/11/06Control Supplement
016725068AP1978/05/26Control Supplement
016725058AP1977/11/22Labeling Revision
016725056AP1977/06/14Labeling Revision
016725055AP1977/06/14Labeling Revision
016725054AP1977/06/14Labeling Revision
016725053AP1977/06/14Labeling Revision
016725049AP1977/07/01Distributor
016725048AP1977/07/01Distributor
016725042AP1975/05/16Labeling Revision
016725040AP1975/05/16Control Supplement
016725037AP1975/05/16Control Supplement
016725034AP1975/05/16Control Supplement
016725031AP1975/05/16Labeling Revision
016725029AP1975/05/16Control Supplement
016725000AP1968/11/08Approval