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 PRESERVATIVE FREE	017029	010	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	1,000 UNITS/ML	Yes	Yes	1972/02/22	1986/04/28	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM IN PLASTIC CONTAINER	017029	013	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	1,000 UNITS/ML	Yes	Yes	1972/02/22	1985/12/05	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM IN PLASTIC CONTAINER	017029	014	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	5,000 UNITS/ML	Yes	Yes	1972/02/22	1985/12/05	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM IN PLASTIC CONTAINER	017029	015	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	10,000 UNITS/ML	Yes	Yes	1972/02/22	1985/12/05	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM IN PLASTIC CONTAINER	017029	016	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	20,000 UNITS/ML	Yes	Yes	1972/02/22	1985/12/05	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM PRESERVATIVE FREE	017029	019	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	10,000 UNITS/ML	Yes	Yes	1972/02/22	2010/11/22	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM	017029	020	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	10,000 UNITS/ML	Yes	Yes	1972/02/22	2011/03/31	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM 20,000 UNITS IN DEXTROSE 5%	017029	021	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	40 UNITS/ML	Yes	Yes	1972/02/22	2017/08/24	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5%	017029	022	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	50 UNITS/ML	Yes	Yes	1972/02/22	2017/08/24	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM 25,000 UNITS IN DEXTROSE 5%	017029	023	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	100 UNITS/ML	Yes	Yes	1972/02/22	2017/08/24	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45%	017029	024	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	50 UNITS/ML	Yes	Yes	1972/02/22	2017/08/24	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM 25,000 UNITS IN SODIUM CHLORIDE 0.45%	017029	025	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	100 UNITS/ML	Yes	Yes	1972/02/22	2017/08/24	FRESENIUS KABI USA	Prescription
HEPARIN SODIUM	017037	001	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	1,000 UNITS/ML	Yes	Yes	1972/03/22	Approved Prior to Jan 1, 1982	HIKMA	Prescription
HEPARIN SODIUM	017037	002	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	5,000 UNITS/ML	Yes	Yes	1972/03/22	Approved Prior to Jan 1, 1982	HIKMA	Prescription
HEPARIN SODIUM	017037	003	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	10,000 UNITS/ML	Yes	Yes	1972/03/22	Approved Prior to Jan 1, 1982	HIKMA	Prescription
HEPARIN SODIUM	017037	013	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	5,000 UNITS/0.5ML	No	No	1972/03/22	1986/04/07	HIKMA	Prescription
HEPARIN SODIUM	017007	001	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	1,000 UNITS/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1974/05/28	Approved Prior to Jan 1, 1982	HIKMA	Discontinued
HEPARIN SODIUM	017007	002	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	5,000 UNITS/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1974/05/28	Approved Prior to Jan 1, 1982	HIKMA	Discontinued
HEPARIN SODIUM	017007	003	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	7,500 UNITS/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1974/05/28	Approved Prior to Jan 1, 1982	HIKMA	Discontinued
HEPARIN SODIUM	017007	004	NDA	HEPARIN SODIUM	INJECTABLE;INJECTION	10,000 UNITS/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1974/05/28	Approved Prior to Jan 1, 1982	HIKMA	Discontinued