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
ANTABUSE	007883	002	NDA	DISULFIRAM	TABLET;ORAL	500MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1951/08/28	Approved Prior to Jan 1, 1982	TEVA WOMENS	Discontinued
ANTABUSE	007883	003	NDA	DISULFIRAM	TABLET;ORAL	250MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1951/08/28	Approved Prior to Jan 1, 1982	TEVA WOMENS	Discontinued
ANTABUSE	088482	001	ANDA	DISULFIRAM	TABLET;ORAL	250MG	Yes	No	1983/12/08	1983/12/08	ODYSSEY PHARMS	Discontinued
ANTABUSE	088483	001	ANDA	DISULFIRAM	TABLET;ORAL	500MG	Yes	No	1983/12/08	1983/12/08	ODYSSEY PHARMS	Discontinued