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
SODIUM BUTABARBITAL	083484	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	15MG	No	No	1973/09/25	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Discontinued
SODIUM BUTABARBITAL	083524	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	16.2MG	No	No	1974/01/15	Approved Prior to Jan 1, 1982	MARSHALL PHARMA	Discontinued
SODIUM BUTABARBITAL	083858	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	32.4MG	No	No	1974/03/14	Approved Prior to Jan 1, 1982	MARSHALL PHARMA	Discontinued
SODIUM BUTABARBITAL	084040	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	30MG	No	No	1974/05/31	Approved Prior to Jan 1, 1982	IVAX SUB TEVA PHARMS	Discontinued
SODIUM BUTABARBITAL	085418	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	15MG	No	No	1977/08/15	Approved Prior to Jan 1, 1982	HIKMA	Discontinued
SODIUM BUTABARBITAL	085432	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	30MG	No	No	1977/12/20	Approved Prior to Jan 1, 1982	HIKMA	Discontinued
SODIUM BUTABARBITAL	085866	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	30MG	No	No	1978/07/20	Approved Prior to Jan 1, 1982	LANNETT	Discontinued
SODIUM BUTABARBITAL	085881	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	100MG	No	No	1978/07/20	Approved Prior to Jan 1, 1982	LANNETT	Discontinued
SODIUM BUTABARBITAL	085849	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	15MG	No	No	1978/08/21	Approved Prior to Jan 1, 1982	LANNETT	Discontinued