药品名称DECLOMYCIN
申请号050261产品号001
活性成分DEMECLOCYCLINE HYDROCHLORIDE市场状态停止上市
剂型或给药途径TABLET;ORAL规格75MG
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构COREPHARMA LLC
化学类型审评分类
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
050261101APLabel2012/09/06下载
050261101APLetter2012/09/07下载
050261100APLetter2008/04/25下载
050261100APLabel2008/06/05下载
050261097APLetter2003/12/22下载
050261095APLetter2003/05/30下载
050261094APLetter2003/12/22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
050261101AP2012/09/05Labeling Revision
050261100AP2008/04/22Labeling Revision
050261097AP2003/12/18Labeling Revision
050261095AP2003/05/01Labeling Revision
050261094AP2003/12/18Labeling Revision
050261093AP2000/12/07Control Supplement
050261092AP1999/10/20Control Supplement
050261091AP1997/06/25Manufacturing Change or Addition
050261090AP1997/06/25Package Change
050261089AP1982/03/26Package Change
050261088AP1980/04/08Control Supplement
050261087AP1979/05/16Control Supplement
050261086AP1978/09/20Formulation Revision
050261085AP1978/09/14Expiration Date Change
050261084AP1978/06/07Labeling Revision
050261083AP1976/08/25Control Supplement
050261082AP1976/06/25Expiration Date Change
050261081AP1976/03/22Control Supplement
050261080AP1975/12/29Control Supplement
050261079AP1975/07/08Control Supplement
050261078AP1974/04/25Expiration Date Change
050261077AP1974/02/28Labeling Revision
050261076AP1974/01/10Formulation Revision
050261075AP1973/10/01Labeling Revision
050261074AP1973/10/01Labeling Revision
050261073AP1973/10/01Labeling Revision
050261072AP1972/02/16Package Change
050261071AP1972/02/16Package Change
050261070AP1972/02/16Labeling Revision
050261069AP1972/01/10Labeling Revision
050261068AP1972/01/10Labeling Revision
050261067AP1972/01/10Labeling Revision
050261066AP1971/07/14Labeling Revision
050261065AP1971/06/14Formulation Revision
050261064AP1970/12/01Formulation Revision
050261063AP1970/10/23Expiration Date Change
050261062AP1970/10/23Expiration Date Change
050261061AP1970/04/14Formulation Revision
050261060AP1969/01/03Package Change
050261059AP1967/12/07Labeling Revision
050261058AP1967/11/17Labeling Revision
050261057AP1967/04/25Labeling Revision
050261056AP1967/04/25Labeling Revision
050261055AP1967/04/25Labeling Revision
050261054AP1967/02/15Labeling Revision
050261053AP1967/02/20Labeling Revision
050261052AP1966/12/29Package Change
050261051AP1966/12/29Package Change
050261050AP1966/11/29Labeling Revision
050261046AP1966/09/28Labeling Revision
050261045AP1966/09/28Labeling Revision
050261044AP1966/12/05Labeling Revision
050261043AP1966/09/15Formulation Revision
050261042AP1966/07/06Labeling Revision
050261041AP1966/06/03Labeling Revision
050261040AP1966/05/04Labeling Revision
050261039AP1966/05/04Labeling Revision
050261038AP1966/05/04Labeling Revision
050261037AP1966/05/04Labeling Revision
050261036AP1966/05/04Labeling Revision
050261035AP1966/05/04Labeling Revision
050261034AP1966/05/04Labeling Revision
050261033AP1966/05/04Labeling Revision
050261032AP1966/05/04Labeling Revision
050261031AP1966/05/04Labeling Revision
050261030AP1966/03/25Labeling Revision
050261029AP1966/03/11Labeling Revision
050261028AP1966/02/18Labeling Revision
050261027AP1966/03/14Labeling Revision
050261026AP1966/01/05Labeling Revision
050261025AP1966/01/05Labeling Revision
050261024AP1965/12/22Labeling Revision
050261023AP1966/01/13Labeling Revision
050261022AP1966/01/13Labeling Revision
050261021AP1965/12/07Labeling Revision
050261020AP1965/12/13Labeling Revision
050261019AP1965/12/23New Dosage Regimen
050261018AP1965/08/19Labeling Revision
050261017AP1965/09/24Package Change
050261016AP1965/05/14Manufacturing Change or Addition
050261015AP1965/05/14Manufacturing Change or Addition
050261014AP1965/03/11Labeling Revision
050261011AP1991/11/20Labeling Revision
050261006AP1987/12/17Formulation Revision
050261005AP1986/10/09Labeling Revision
050261003AP1965/02/10Labeling Revision
050261002AP1983/06/21Control Supplement
050261000AP1964/09/22Approval