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
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	062414	004	ANDA	GENTAMICIN SULFATE	INJECTABLE;INJECTION	EQ 1.8MG BASE/ML	No	No	1983/08/15	1983/08/15	HOSPIRA	Discontinued
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	062414	005	ANDA	GENTAMICIN SULFATE	INJECTABLE;INJECTION	EQ 2MG BASE/ML	No	No	1983/08/15	1983/08/15	HOSPIRA	Discontinued
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	062414	006	ANDA	GENTAMICIN SULFATE	INJECTABLE;INJECTION	EQ 60MG BASE/100ML	No	No	1983/08/15	1983/08/15	HOSPIRA	Discontinued
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	062414	007	ANDA	GENTAMICIN SULFATE	INJECTABLE;INJECTION	EQ 70MG BASE/100ML	No	No	1983/08/15	1983/08/15	HOSPIRA	Discontinued
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	062414	008	ANDA	GENTAMICIN SULFATE	INJECTABLE;INJECTION	EQ 80MG BASE/100ML	No	No	1983/08/15	1983/08/15	HOSPIRA	Discontinued
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	062414	009	ANDA	GENTAMICIN SULFATE	INJECTABLE;INJECTION	EQ 90MG BASE/100ML	No	No	1983/08/15	1983/08/15	HOSPIRA	Discontinued
GENTAMICIN SULFATE IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	062414	010	ANDA	GENTAMICIN SULFATE	INJECTABLE;INJECTION	EQ 100MG BASE/100ML	No	No	1983/08/15	1983/08/15	HOSPIRA	Discontinued
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
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 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
BACTERIOSTATIC SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	088911	001	ANDA	SODIUM CHLORIDE	SOLUTION;INJECTION	270MG/30ML (9MG/ML)	No	No	1985/02/07	1985/02/07	FRESENIUS KABI USA	Prescription
BACTERIOSTATIC SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	088911	002	ANDA	SODIUM CHLORIDE	SOLUTION;INJECTION	90MG/10ML (9MG/ML)	No	No	1985/02/07	1985/05/17	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM 1,000 UNITS IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER	019042	001	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	200 UNITS/100ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	No	No	1985/03/29	1985/03/29	B BRAUN	Discontinued