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
ZEFAZONE	050637	001	NDA	CEFMETAZOLE SODIUM	INJECTABLE;INJECTION	EQ 1GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1989/12/11	1989/12/11	PHARMACIA AND UPJOHN	Discontinued
ZEFAZONE	050637	002	NDA	CEFMETAZOLE SODIUM	INJECTABLE;INJECTION	EQ 2GM BASE/VIAL Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1989/12/11	1989/12/11	PHARMACIA AND UPJOHN	Discontinued
ZEFAZONE IN PLASTIC CONTAINER	050683	001	NDA	CEFMETAZOLE SODIUM	INJECTABLE;INJECTION	EQ 20MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1992/12/29	1992/12/29	PHARMACIA AND UPJOHN	Discontinued
ZEFAZONE IN PLASTIC CONTAINER	050683	002	NDA	CEFMETAZOLE SODIUM	INJECTABLE;INJECTION	EQ 40MG BASE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	Yes	No	1992/12/29	1992/12/29	PHARMACIA AND UPJOHN	Discontinued