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
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	018916	009	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	5,000 UNITS/100ML	No	No	1984/01/31	1984/01/31	HOSPIRA	Discontinued
HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	018916	010	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	200 UNITS/100ML	Yes	Yes	1984/01/31	1989/06/23	HOSPIRA	Prescription
HEPARIN SODIUM 2,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	018916	011	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	200 UNITS/100ML	Yes	Yes	1984/01/31	1989/06/23	HOSPIRA	Prescription
CEPHALOTHIN SODIUM W/ SODIUM CHLORIDE IN PLASTIC CONTAINER	062422	001	ANDA	CEPHALOTHIN SODIUM	INJECTABLE;INJECTION	EQ 20MG BASE/ML	No	No	1984/01/31	1984/01/31	BAXTER HLTHCARE	Discontinued
CEPHALOTHIN SODIUM W/ SODIUM CHLORIDE IN PLASTIC CONTAINER	062422	002	ANDA	CEPHALOTHIN SODIUM	INJECTABLE;INJECTION	EQ 40MG BASE/ML	No	No	1984/01/31	1984/01/31	BAXTER HLTHCARE	Discontinued
SODIUM CHLORIDE 0.9% IN PLASTIC THERMOJECT KIT FOR CARDIAC OUTPUT USE	019217	001	NDA	SODIUM CHLORIDE	SOLUTION;INJECTION	90MG/10ML (9MG/ML)	Yes	No	1984/07/13	1984/07/13	ICU MEDICAL INC	Discontinued
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	019217	002	NDA	SODIUM CHLORIDE	SOLUTION;INJECTION	45MG/5ML (9MG/ML)	Yes	No	1984/07/13	1998/11/18	ICU MEDICAL INC	Discontinued
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	019217	003	NDA	SODIUM CHLORIDE	SOLUTION;INJECTION	90MG/10ML (9MG/ML)	Yes	No	1984/07/13	1998/11/18	ICU MEDICAL INC	Discontinued
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	019217	004	NDA	SODIUM CHLORIDE	SOLUTION;INJECTION	360MG/40ML (9MG/ML)	Yes	No	1984/07/13	1999/04/01	ICU MEDICAL INC	Discontinued
SODIUM CHLORIDE 14.6%	018897	001	NDA	SODIUM CHLORIDE	SOLUTION;INTRAVENOUS	50MEQ/20ML (2.5MEQ/ML) Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1984/07/20	1984/07/20	HOSPIRA	Discontinued
SODIUM CHLORIDE 14.6%	018897	002	NDA	SODIUM CHLORIDE	SOLUTION;INTRAVENOUS	100MEQ/40ML (2.5MEQ/ML)	Yes	Yes	1984/07/20	1984/07/20	HOSPIRA	Prescription
SODIUM CHLORIDE 23.4%	018897	003	NDA	SODIUM CHLORIDE	SOLUTION;INTRAVENOUS	400MEQ/100ML (4MEQ/ML)	Yes	Yes	1984/07/20	2020/06/18	HOSPIRA	Prescription
AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER	018924	001	NDA	AMINOPHYLLINE	INJECTABLE;INJECTION	100MG/100ML	No	No	1984/12/12	1984/12/12	HOSPIRA	Discontinued
AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER	018924	002	NDA	AMINOPHYLLINE	INJECTABLE;INJECTION	200MG/100ML	No	No	1984/12/12	1984/12/12	HOSPIRA	Discontinued
AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER	018924	003	NDA	AMINOPHYLLINE	INJECTABLE;INJECTION	400MG/100ML	No	No	1984/12/12	1984/12/12	HOSPIRA	Discontinued
AMINOPHYLLINE IN SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER	018924	004	NDA	AMINOPHYLLINE	INJECTABLE;INJECTION	500MG/100ML	No	No	1984/12/12	1984/12/12	HOSPIRA	Discontinued
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	088912	001	ANDA	SODIUM CHLORIDE	SOLUTION;INJECTION	90MG/10ML (9MG/ML)	No	Yes	1985/01/10	1985/01/10	FRESENIUS KABI USA	Prescription
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	088912	002	ANDA	SODIUM CHLORIDE	SOLUTION;INJECTION	180MG/20ML (9MG/ML)	No	Yes	1985/01/10	1985/01/10	FRESENIUS KABI USA	Prescription
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	088912	003	ANDA	SODIUM CHLORIDE	SOLUTION;INJECTION	270MG/30ML (9MG/ML)	No	Yes	1985/01/10	1985/01/10	FRESENIUS KABI USA	Prescription
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	088912	004	ANDA	SODIUM CHLORIDE	SOLUTION;INJECTION	18MG/2ML (9MG/ML)	No	Yes	1985/01/10	1985/11/29	FRESENIUS KABI USA	Prescription