TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER(CIMETIDINE HYDROCHLORIDE)

药品名称	TAGAMET HYDROCHLORIDE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
申请号	019434	产品号	001
活性成分	CIMETIDINE HYDROCHLORIDE	市场状态	停止上市
剂型或给药途径	INJECTABLE;INJECTION	规格	EQ 6MG BASE/ML
治疗等效代码		参比药物	否
批准日期	1985/10/31	申请机构	GLAXOSMITHKLINE
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
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历史专利信息
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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
019434	030	AP	1998/01/08	Manufacturing Change or Addition
019434	029	AP	1997/04/15	Control Supplement
019434	028	AP	1994/12/06	Manufacturing Change or Addition
019434	027	AP	1995/02/22	Labeling Revision
019434	026	AP	1993/11/10	Manufacturing Change or Addition
019434	025	AP	1993/09/13	Manufacturing Change or Addition
019434	024	AP	1993/06/08	Manufacturing Change or Addition
019434	022	AP	1996/10/23	Package Change
019434	021	AP	1992/06/04	Control Supplement
019434	020	AP	1992/07/16	Control Supplement
019434	019	AP	1992/01/07	Labeling Revision
019434	018	AP	1992/08/27	Control Supplement
019434	016	AP	1992/01/30	Control Supplement
019434	015	AP	1991/05/23	Control Supplement
019434	014	AP	1991/11/13	Labeling Revision
019434	013	AP	1989/11/13	Labeling Revision
019434	011	AP	1990/05/30	Control Supplement
019434	010	AP	1991/03/07	Labeling Revision
019434	009	AP	1989/06/26	Labeling Revision
019434	008	AP	1989/03/20	Manufacturing Change or Addition
019434	007	AP	1989/06/26	Labeling Revision
019434	005	AP	1988/06/15	Labeling Revision
019434	004	AP	1988/05/20	Labeling Revision
019434	003	AP	1988/03/31	New Dosage Regimen
019434	002	AP	1986/04/29	Labeling Revision
019434	001	AP	1986/04/23	Labeling Revision
019434	000	AP	1985/10/31	Approval