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
CORTEF ACETATE	009378	002	NDA	HYDROCORTISONE ACETATE	INJECTABLE;INJECTION	50MG/ML	No	No	--	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
CORTEF	009864	001	NDA	HYDROCORTISONE	INJECTABLE;INJECTION	50MG/ML	No	No	--	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
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-DELTA-CORTEF	061037	001	ANDA	NEOMYCIN SULFATE; PREDNISOLONE ACETATE	SUSPENSION/DROPS;OPHTHALMIC	EQ 3.5MG BASE/ML;0.25%	No	No	--	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
NEO-DELTA-CORTEF	061039	001	ANDA	NEOMYCIN SULFATE; PREDNISOLONE ACETATE	OINTMENT;OPHTHALMIC	EQ 3.5MG BASE/GM;0.5%	No	No	--	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
NEO-DELTA-CORTEF	061039	002	ANDA	NEOMYCIN SULFATE; PREDNISOLONE ACETATE	OINTMENT;OPHTHALMIC	EQ 3.5MG BASE/GM;0.25%	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
CORTEF	008697	001	NDA	HYDROCORTISONE	TABLET;ORAL	10MG	Yes	No	1952/12/15	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Prescription
CORTEF	008697	002	NDA	HYDROCORTISONE	TABLET;ORAL	20MG	Yes	Yes	1952/12/15	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Prescription
CORTEF	008697	003	NDA	HYDROCORTISONE	TABLET;ORAL	5MG	Yes	No	1952/12/15	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Prescription
CORTEF ACETATE	008917	001	NDA	HYDROCORTISONE ACETATE	OINTMENT;TOPICAL	2.5% Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1953/07/28	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
CORTEF ACETATE	008917	002	NDA	HYDROCORTISONE ACETATE	OINTMENT;TOPICAL	1%	No	No	1953/07/28	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Discontinued
SOLU-CORTEF	009866	001	NDA	HYDROCORTISONE SODIUM SUCCINATE	INJECTABLE;INJECTION	EQ 100MG BASE/VIAL	Yes	Yes	1955/04/27	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Prescription
SOLU-CORTEF	009866	002	NDA	HYDROCORTISONE SODIUM SUCCINATE	INJECTABLE;INJECTION	EQ 250MG BASE/VIAL	Yes	Yes	1955/04/27	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Prescription
SOLU-CORTEF	009866	003	NDA	HYDROCORTISONE SODIUM SUCCINATE	INJECTABLE;INJECTION	EQ 500MG BASE/VIAL	Yes	Yes	1955/04/27	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Prescription
SOLU-CORTEF	009866	004	NDA	HYDROCORTISONE SODIUM SUCCINATE	INJECTABLE;INJECTION	EQ 1GM BASE/VIAL	Yes	Yes	1955/04/27	Approved Prior to Jan 1, 1982	PHARMACIA AND UPJOHN	Prescription