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
ZINACEF	050558	002	NDA	CEFUROXIME SODIUM	INJECTABLE;INTRAMUSCULAR, INTRAVENOUS	EQ 750MG BASE/VIAL	Yes	No	1983/10/19	1983/10/19	PAI HOLDINGS PHARM	Discontinued
ZINACEF	050558	003	NDA	CEFUROXIME SODIUM	INJECTABLE;INJECTION	EQ 1.5GM BASE/VIAL	Yes	No	1983/10/19	1983/10/19	PAI HOLDINGS PHARM	Discontinued
ZINACEF	050558	004	NDA	CEFUROXIME SODIUM	INJECTABLE;INJECTION	EQ 7.5GM BASE/VIAL	Yes	No	1983/10/19	1986/10/23	PAI HOLDINGS PHARM	Discontinued
ZINACEF IN PLASTIC CONTAINER	050643	001	NDA	CEFUROXIME SODIUM	INJECTABLE;INJECTION	EQ 15MG BASE/ML	No	No	1989/04/28	1989/04/28	PAI HOLDINGS PHARM	Discontinued
ZINACEF IN PLASTIC CONTAINER	050643	002	NDA	CEFUROXIME SODIUM	INJECTABLE;INJECTION	EQ 30MG BASE/ML	Yes	No	1989/04/28	1989/04/28	PAI HOLDINGS PHARM	Discontinued