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
DELTASONE	009986	002	NDA	PREDNISONE	TABLET;ORAL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1955/06/21	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
DELTASONE	009986	005	NDA	PREDNISONE	TABLET;ORAL	2.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1955/06/21	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
DELTASONE	009986	006	NDA	PREDNISONE	TABLET;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1955/06/21	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
DELTASONE	009986	007	NDA	PREDNISONE	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1955/06/21	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
DELTASONE	009986	008	NDA	PREDNISONE	TABLET;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1955/06/21	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued