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
HYDROCORTISONE AND ACETIC ACID	040097	001	ANDA	ACETIC ACID, GLACIAL; HYDROCORTISONE	SOLUTION/DROPS;OTIC	2%;1%	No	No	--	1994/10/31	BAUSCH AND LOMB	Discontinued
BACITRACIN-NEOMYCIN-POLYMYXIN W/ HYDROCORTISONE ACETATE	060731	002	ANDA	BACITRACIN; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE	OINTMENT;OPHTHALMIC	400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM	No	No	--	Approved Prior to Jan 1, 1982	ALTANA	Discontinued
NEOMYCIN & POLYMYXIN B SULFATES & BACITRACIN ZINC & HYDROCORTISONE	062381	001	ANDA	BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE	OINTMENT;TOPICAL	400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM	No	No	--	1985/09/06	PHARMAFAIR	Discontinued
ZINC BACITRACIN,NEOMYCIN SULFATE,POLYMYXIN B SULFATE & HYDROCORTISONE	062389	001	ANDA	BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE	OINTMENT;OPHTHALMIC	400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM	No	No	--	1982/07/02	PHARMAFAIR	Discontinued
NEOMYCIN SULFATE-POLYMYXIN B SULFATE-HYDROCORTISONE	062394	001	ANDA	HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE	SOLUTION/DROPS;OTIC	1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML	No	No	--	1982/09/29	PHARMAFAIR	Discontinued
NEOMYCIN SULFATE, POLYMYXIN B SULFATE & HYDROCORTISONE	062617	001	ANDA	HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE	SUSPENSION/DROPS;OTIC	1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML	No	No	--	1985/09/18	PHARMAFAIR	Discontinued
NEOMYCIN SULFATE-POLYMYXIN B SULFATE-HYDROCORTISONE	062623	001	ANDA	HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE	SUSPENSION/DROPS;OPHTHALMIC	1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML	No	No	--	1985/09/24	PHARMAFAIR	Discontinued
HYDROCORTISONE	080395	001	ANDA	HYDROCORTISONE	TABLET;ORAL	20MG	No	No	--	Approved Prior to Jan 1, 1982	PUREPAC PHARM	Discontinued
HYDROCORTISONE ACETATE	080419	001	ANDA	HYDROCORTISONE ACETATE	CREAM;TOPICAL	1%	No	No	--	1982/01/25	CENCI	Discontinued
HYDROCORTISONE	080452	001	ANDA	HYDROCORTISONE	CREAM;TOPICAL	0.5%	No	No	--	Approved Prior to Jan 1, 1982	EVERYLIFE	Discontinued
HYDROCORTISONE	080452	002	ANDA	HYDROCORTISONE	CREAM;TOPICAL	1%	No	No	--	Approved Prior to Jan 1, 1982	EVERYLIFE	Discontinued
HYDROCORTISONE	080456	002	ANDA	HYDROCORTISONE	CREAM;TOPICAL	0.5%	No	No	--	Approved Prior to Jan 1, 1982	INGRAM PHARM	Discontinued
HYDROCORTISONE	080456	003	ANDA	HYDROCORTISONE	CREAM;TOPICAL	1%	No	No	--	Approved Prior to Jan 1, 1982	INGRAM PHARM	Discontinued
HYDROCORTISONE	080489	002	ANDA	HYDROCORTISONE	OINTMENT;TOPICAL	0.5%	No	No	--	Approved Prior to Jan 1, 1982	ALTANA	Discontinued
HYDROCORTISONE	080489	003	ANDA	HYDROCORTISONE	OINTMENT;TOPICAL	1%	No	No	--	Approved Prior to Jan 1, 1982	ALTANA	Discontinued
HYDROCORTISONE	080624	001	ANDA	HYDROCORTISONE	TABLET;ORAL	20MG	No	No	--	Approved Prior to Jan 1, 1982	ELKINS SINN	Discontinued
HYDROCORTISONE	080732	001	ANDA	HYDROCORTISONE	TABLET;ORAL	20MG	No	No	--	Approved Prior to Jan 1, 1982	INWOOD LABS	Discontinued
HYDROCORTISONE	080781	001	ANDA	HYDROCORTISONE	TABLET;ORAL	20MG	No	No	--	Approved Prior to Jan 1, 1982	IMPAX LABS	Discontinued
HYDROCORTISONE	080848	002	ANDA	HYDROCORTISONE	CREAM;TOPICAL	0.5%	No	No	--	Approved Prior to Jan 1, 1982	ALTANA	Discontinued
HYDROCORTISONE	080848	003	ANDA	HYDROCORTISONE	CREAM;TOPICAL	1%	No	No	--	Approved Prior to Jan 1, 1982	ALTANA	Discontinued