药品名称HEPARIN SODIUM
申请号004570产品号002
活性成分HEPARIN SODIUM市场状态停止上市
剂型或给药途径INJECTABLE;INJECTION规格5,000 UNITS/ML
治疗等效代码参比药物
批准日期Approved Prior to Jan 1, 1982申请机构PHARMACIA AND UPJOHN CO
化学类型审评分类
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历史专利信息
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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
004570056AP2000/04/03Manufacturing Change or Addition
004570055AP1999/09/15Labeling Revision
004570054AP1996/03/04Labeling Revision
004570053AP1996/01/31Manufacturing Change or Addition
004570052AP1991/07/09Control Supplement
004570051AP1988/11/16Labeling Revision
004570050AP1988/08/12Labeling Revision
004570049AP1990/01/29Control Supplement
004570048AP1987/07/24Labeling Revision
004570047AP1987/01/21Labeling Revision
004570046AP1988/01/29Control Supplement
004570045AP1983/03/25Labeling Revision
004570044AP1983/01/21Labeling Revision
004570043AP1986/10/24Practioner Draft Labeling
004570042AP1981/08/19Labeling Revision
004570041AP1981/06/02Labeling Revision
004570040AP1981/02/04Labeling Revision
004570039AP1981/01/14Labeling Revision
004570038AP1980/12/03Package Change
004570037AP1980/08/20Control Supplement
004570036AP1980/10/14Package Change
004570035AP1981/02/18Labeling Revision
004570034AP1980/02/05Formulation Revision
004570033AP1981/06/02Labeling Revision
004570032AP1980/02/05Control Supplement
004570031AP1980/02/05Package Change
004570029AP1978/10/04Control Supplement
004570026AP1978/02/02Control Supplement
004570023AP1977/02/11Formulation Revision
004570022AP1976/02/24Labeling Revision
004570021AP1976/02/24Labeling Revision
004570020AP1976/07/09Package Change
004570019AP1975/08/14Labeling Revision
004570018AP1975/08/14Control Supplement
004570000AP1942/02/05Approval