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
72603-351-25	72603-351	HUMAN PRESCRIPTION DRUG	CUPRIC CHLORIDE	CUPRIC CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20241001	N/A	ANDA	ANDA217626	Northstar Rx LLC	CUPRIC CHLORIDE	.4 mg/mL	25 VIAL, SINGLE-DOSE in 1 PACKAGE (72603-351-25) / 10 mL in 1 VIAL, SINGLE-DOSE (72603-351-01)
84897-013-25	84897-013	HUMAN PRESCRIPTION DRUG	CUPRIC CHLORIDE	CUPRIC CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20260507	N/A	ANDA	ANDA217626	Renova Pharmaceuticals LLC	CUPRIC CHLORIDE	.4 mg/mL	25 VIAL, SINGLE-DOSE in 1 PACKAGE (84897-013-25) / 10 mL in 1 VIAL, SINGLE-DOSE (84897-013-01)
72819-234-16	72819-234	HUMAN PRESCRIPTION DRUG	CUPRIC CHLORIDE	CUPRIC CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20240705	N/A	ANDA	ANDA217626	Archis Pharma LLC	CUPRIC CHLORIDE	.4 mg/mL	25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-16) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-06)
72819-234-99	72819-234	HUMAN PRESCRIPTION DRUG	CUPRIC CHLORIDE	CUPRIC CHLORIDE	INJECTION, SOLUTION	INTRAVENOUS	20241001	N/A	ANDA	ANDA217626	Archis Pharma LLC	CUPRIC CHLORIDE	.4 mg/mL	25 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-99) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-96)