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
NEO-CORTEF	060610	001	ANDA	HYDROCORTISONE ACETATE; NEOMYCIN SULFATE	OINTMENT;OPHTHALMIC	0.5%;EQ 3.5MG BASE/GM	No	No	--	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
NEO-CORTEF	060610	002	ANDA	HYDROCORTISONE ACETATE; NEOMYCIN SULFATE	OINTMENT;OPHTHALMIC	1.5%;EQ 3.5MG BASE/GM	No	No	--	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
NEO-CORTEF	060612	001	ANDA	HYDROCORTISONE ACETATE; NEOMYCIN SULFATE	SUSPENSION/DROPS;OPHTHALMIC	1.5%;EQ 3.5MG BASE/ML	No	No	--	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
NEO-CORTEF	060612	002	ANDA	HYDROCORTISONE ACETATE; NEOMYCIN SULFATE	SUSPENSION/DROPS;OPHTHALMIC	0.5%;EQ 3.5MG BASE/ML	No	No	--	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
NEO-CORTEF	061049	001	ANDA	HYDROCORTISONE ACETATE; NEOMYCIN SULFATE	CREAM;TOPICAL	1%;EQ 3.5MG BASE/GM	No	No	--	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
NEO-CORTEF	061049	002	ANDA	HYDROCORTISONE ACETATE; NEOMYCIN SULFATE	CREAM;TOPICAL	2.5%;EQ 3.5MG BASE/GM	No	No	--	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
NEO-CORTEF	060751	001	ANDA	HYDROCORTISONE ACETATE; NEOMYCIN SULFATE	OINTMENT;TOPICAL	0.5%;EQ 3.5MG BASE/GM	No	No	1965/05/18	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
NEO-CORTEF	060751	002	ANDA	HYDROCORTISONE ACETATE; NEOMYCIN SULFATE	OINTMENT;TOPICAL	1%;EQ 3.5MG BASE/GM	No	No	1965/05/18	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
NEO-CORTEF	060751	003	ANDA	HYDROCORTISONE ACETATE; NEOMYCIN SULFATE	OINTMENT;TOPICAL	2.5%;EQ 3.5MG BASE/GM	No	No	1965/05/18	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued