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
BUTISOL SODIUM	000793	002	NDA	BUTABARBITAL SODIUM	TABLET;ORAL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1939/06/05	Approved Prior to Jan 1, 1982	NORVIUM BIOSCIENCE	Discontinued
BUTISOL SODIUM	000793	003	NDA	BUTABARBITAL SODIUM	TABLET;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1939/06/05	Approved Prior to Jan 1, 1982	NORVIUM BIOSCIENCE	Discontinued
BUTISOL SODIUM	000793	004	NDA	BUTABARBITAL SODIUM	TABLET;ORAL	30MG	Yes	No	1939/06/05	Approved Prior to Jan 1, 1982	NORVIUM BIOSCIENCE	Discontinued
BUTISOL SODIUM	000793	005	NDA	BUTABARBITAL SODIUM	TABLET;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1939/06/05	Approved Prior to Jan 1, 1982	NORVIUM BIOSCIENCE	Discontinued
BUTISOL SODIUM	085380	001	ANDA	BUTABARBITAL SODIUM	ELIXIR;ORAL	30MG/5ML	No	No	1978/04/10	Approved Prior to Jan 1, 1982	MEDA PHARMS	Discontinued