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
DIPROSONE	017829	001	NDA	BETAMETHASONE DIPROPIONATE	DISC;TOPICAL	EQ 0.1% BASE	No	No	--	Approved Prior to Jan 1, 1982	SCHERING	Discontinued
DIPROSONE	017536	001	NDA	BETAMETHASONE DIPROPIONATE	CREAM;TOPICAL	EQ 0.05% BASE	No	No	1975/01/29	Approved Prior to Jan 1, 1982	SCHERING	Discontinued
DIPROSONE	017691	001	NDA	BETAMETHASONE DIPROPIONATE	OINTMENT;TOPICAL	EQ 0.05% BASE	No	No	1976/04/15	Approved Prior to Jan 1, 1982	SCHERING	Discontinued
DIPROSONE	017781	001	NDA	BETAMETHASONE DIPROPIONATE	LOTION;TOPICAL	EQ 0.05% BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1977/02/01	Approved Prior to Jan 1, 1982	SCHERING	Discontinued