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
CELESTONE	014762	001	NDA	BETAMETHASONE	CREAM;TOPICAL	0.2%	No	No	--	Approved Prior to Jan 1, 1982	SCHERING	Discontinued
CELESTONE	012657	003	NDA	BETAMETHASONE	TABLET;ORAL	0.6MG	No	No	1961/04/17	Approved Prior to Jan 1, 1982	SCHERING	Discontinued
CELESTONE	014215	002	NDA	BETAMETHASONE	SYRUP;ORAL	0.6MG/5ML	No	No	1964/04/13	Approved Prior to Jan 1, 1982	MERCK SHARP DOHME	Discontinued
CELESTONE SOLUSPAN	014602	001	NDA	BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE	INJECTABLE;INJECTION	3MG/ML;EQ 3MG BASE/ML	Yes	Yes	1965/03/03	Approved Prior to Jan 1, 1982	ORGANON	Prescription
CELESTONE	017561	001	NDA	BETAMETHASONE SODIUM PHOSPHATE	INJECTABLE;INJECTION	EQ 3MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1974/12/31	Approved Prior to Jan 1, 1982	SCHERING	Discontinued