美国FDA药品数据库-药物在线

商品名	申请号	产品号	申请类型	活性成分	剂型/给药途径	规格/剂量	RLD	RS	申请号原始批准/暂定批准日期	产品号批准日期	申请人	市场状态
SULFADIAZINE	004125	005	NDA	SULFADIAZINE	TABLET;ORAL	300MG	No	No	--	Approved Prior to Jan 1, 1982	ABBVIE	Discontinued
SULFADIAZINE	080081	001	ANDA	SULFADIAZINE	TABLET;ORAL	500MG	Yes	No	--	Approved Prior to Jan 1, 1982	IMPAX LABS	Discontinued
SULFADIAZINE	080088	001	ANDA	SULFADIAZINE	TABLET;ORAL	500MG	No	No	--	Approved Prior to Jan 1, 1982	EVERYLIFE	Discontinued
SULFADIAZINE	004054	001	NDA	SULFADIAZINE	TABLET;ORAL	500MG	No	No	1941/08/11	Approved Prior to Jan 1, 1982	LEDERLE	Discontinued
SULFADIAZINE SODIUM	004054	002	NDA	SULFADIAZINE SODIUM	INJECTABLE;INJECTION	250MG/ML	No	No	1941/08/11	Approved Prior to Jan 1, 1982	LEDERLE	Discontinued
SULFADIAZINE	004122	002	NDA	SULFADIAZINE	TABLET;ORAL	500MG	Yes	No	1941/08/26	Approved Prior to Jan 1, 1982	LILLY	Discontinued
SULFADIAZINE	080084	001	ANDA	SULFADIAZINE	TABLET;ORAL	500MG	No	No	1978/07/05	Approved Prior to Jan 1, 1982	CHARTWELL MOLECULAR	Discontinued
SULFADIAZINE	040091	001	ANDA	SULFADIAZINE	TABLET;ORAL	500MG	No	Yes	1994/07/29	1994/07/29	EPIC PHARMA LLC	Prescription