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
HYDROCORTONE	009018	003	NDA	HYDROCORTISONE ACETATE	OINTMENT;OPHTHALMIC, OTIC	1.5%	No	No	--	Approved Prior to Jan 1, 1982	MERCK	Discontinued
HYDROCORTONE	008228	001	NDA	HYDROCORTISONE ACETATE	INJECTABLE;INJECTION	25MG/ML	No	No	1951/12/21	Approved Prior to Jan 1, 1982	MERCK	Discontinued
HYDROCORTONE	008228	004	NDA	HYDROCORTISONE ACETATE	INJECTABLE;INJECTION	50MG/ML	No	No	1951/12/21	Approved Prior to Jan 1, 1982	MERCK	Discontinued
HYDROCORTONE	008506	007	NDA	HYDROCORTISONE	TABLET;ORAL	10MG	No	No	1952/08/05	Approved Prior to Jan 1, 1982	MERCK	Discontinued
HYDROCORTONE	008506	011	NDA	HYDROCORTISONE	TABLET;ORAL	20MG	No	No	1952/08/05	Approved Prior to Jan 1, 1982	MERCK	Discontinued
HYDROCORTONE	012052	001	NDA	HYDROCORTISONE SODIUM PHOSPHATE	INJECTABLE;INJECTION	EQ 50MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1960/06/08	Approved Prior to Jan 1, 1982	MERCK	Discontinued