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	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
BUTABARBITAL SODIUM	085383	001	ANDA	BUTABARBITAL SODIUM	ELIXIR;ORAL	30MG/5ML	No	No	1979/02/26	Approved Prior to Jan 1, 1982	WOCKHARDT	Discontinued
BUTABARBITAL SODIUM	085934	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	30MG	No	No	1994/09/16	Approved Prior to Jan 1, 1982	SANDOZ	Discontinued
BUTABARBITAL SODIUM	085938	001	ANDA	BUTABARBITAL SODIUM	TABLET;ORAL	15MG	Yes	No	1994/09/16	Approved Prior to Jan 1, 1982	SANDOZ	Discontinued