美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
67184-1005-2	67184-1005	HUMAN PRESCRIPTION DRUG	Ceftriaxone Sodium	Ceftriaxone Sodium	INJECTION, POWDER, FOR SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20160629	N/A	ANDA	ANDA203702	Qilu Pharmaceutical Co., Ltd.	CEFTRIAXONE SODIUM	250 mg/1	1 VIAL, SINGLE-USE in 1 CARTON (67184-1005-2) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
85766-128-01	85766-128	HUMAN PRESCRIPTION DRUG	Ceftriaxone Sodium	Ceftriaxone Sodium	INJECTION, POWDER, FOR SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20251203	N/A	ANDA	ANDA203702	Sportpharm LLC	CEFTRIAXONE SODIUM	500 mg/1	1 VIAL, SINGLE-USE in 1 CARTON (85766-128-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE
85766-128-10	85766-128	HUMAN PRESCRIPTION DRUG	Ceftriaxone Sodium	Ceftriaxone Sodium	INJECTION, POWDER, FOR SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20251203	N/A	ANDA	ANDA203702	Sportpharm LLC	CEFTRIAXONE SODIUM	500 mg/1	10 VIAL, SINGLE-USE in 1 CARTON (85766-128-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE