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
52268-302-01	52268-302	HUMAN PRESCRIPTION DRUG	NuLYTELY	polyethylene glycol 3350, sodium chloride, sodium bicarbonate and potassium chloride	POWDER, FOR SOLUTION	ORAL	19910422	20240831	NDA	NDA019797	Braintree Laboratories, Inc.	POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE	420 g/4L; 1.48 g/4L; 5.72 g/4L; 11.2 g/4L	4 L in 1 PACKAGE (52268-302-01)
10572-302-01	10572-302	HUMAN PRESCRIPTION DRUG	PEG-3350, sodium chloride, sodium bicarbonate and potassium chloride	polyethylene glycol 3350, sodium chloride, sodium bicarbonate, potassium chloride	POWDER, FOR SOLUTION	ORAL	20130301	N/A	NDA AUTHORIZED GENERIC	NDA019797	Affordable Pharmaceuticals, LLC	POLYETHYLENE GLYCOL 3350; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE	420 g/4L; 1.48 g/4L; 5.72 g/4L; 11.2 g/4L	4 L in 1 BOTTLE (10572-302-01)