药品名称CLEOCIN T
申请号050537产品号001
活性成分CLINDAMYCIN PHOSPHATE市场状态处方药
剂型或给药途径SOLUTION;TOPICAL规格EQ 1% BASE
治疗等效代码AT参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PHARMACIA AND UPJOHN CO
化学类型New dosage form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
050537037APLetter2016/01/20下载
050537037APLabel2016/01/26下载
050537035APLetter2014/04/07下载
050537035APLabel2014/04/08下载
050537026APLetter2003/06/08下载
050537026APLabel2003/06/08下载
050537013APLetter2002/07/14下载
050537013APLabel2002/07/14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
050537037AP2016/01/15Labeling Revision
050537036AP2014/08/29Manufacturing Change or Addition
050537035AP2014/04/04Labeling Revision
050537026AP2003/05/30Labeling Revision
050537024AP1999/06/07Manufacturing Change or Addition
050537023AP1994/09/05Manufacturing Change or Addition
050537022AP1981/08/21Expiration Date Change
050537021AP1982/02/25Labeling Revision
050537019AP1981/11/23Labeling Revision
050537018AP1981/11/18Labeling Revision
050537016AP1992/12/21Package Change
050537014AP1994/02/22Control Supplement
050537013AP2002/07/14Labeling Revision
050537011AP1989/07/28Package Change
050537010AP1989/03/15Labeling Revision
050537009AP1981/04/20Labeling Revision
050537008AP1981/05/11Labeling Revision
050537007AP1986/01/23Control Supplement
050537006AP1984/08/06Labeling Revision
050537005AP1986/07/18Labeling Revision
050537004AP1983/03/02Labeling Revision
050537003AP1980/09/30Manufacturing Change or Addition
050537002AP1980/09/15Manufacturing Change or Addition
050537001AP1980/08/14Labeling Revision
050537000AP1980/07/09Approval