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
85592-819-30	85592-819	HUMAN PRESCRIPTION DRUG	LACTULOSE Crystalline	lactulose	POWDER, FOR SOLUTION	ORAL	20250901	N/A	ANDA	ANDA074712	Cumberland Assured Products Inc.	LACTULOSE	10 g/10g	30 POUCH in 1 CARTON (85592-819-30) / 10 g in 1 POUCH (85592-819-01)
66220-729-30	66220-729	HUMAN PRESCRIPTION DRUG	KRISTALOSE	lactulose	POWDER, FOR SOLUTION	ORAL	20120120	N/A	ANDA	ANDA074712	Cumberland Pharmaceuticals Inc.	LACTULOSE	20 g/20g	30 POUCH in 1 CARTON (66220-729-30) / 20 g in 1 POUCH (66220-729-01)
69067-020-15	69067-020	HUMAN PRESCRIPTION DRUG	Lactulose	Lactulose	SOLUTION	ORAL	20250207	N/A	ANDA	ANDA074712	Foxland Pharmaceuticals, Inc.	LACTULOSE	20 g/20g	15 PACKET in 1 CARTON (69067-020-15) / 20 g in 1 PACKET
66220-719-30	66220-719	HUMAN PRESCRIPTION DRUG	KRISTALOSE	lactulose	POWDER, FOR SOLUTION	ORAL	20120120	N/A	ANDA	ANDA074712	Cumberland Pharmaceuticals Inc.	LACTULOSE	10 g/10g	30 POUCH in 1 CARTON (66220-719-30) / 10 g in 1 POUCH (66220-719-01)
69067-010-15	69067-010	HUMAN PRESCRIPTION DRUG	Lactulose	Lactulose	SOLUTION	ORAL	20180921	N/A	ANDA	ANDA074712	Foxland Pharmaceuticals, Inc.	LACTULOSE	10 g/10g	15 POUCH in 1 CARTON (69067-010-15) / 10 g in 1 POUCH
85592-829-30	85592-829	HUMAN PRESCRIPTION DRUG	LACTULOSE Crystalline	lactulose	POWDER, FOR SOLUTION	ORAL	20250901	N/A	ANDA	ANDA074712	Cumberland Assured Products Inc.	LACTULOSE	20 g/20g	30 POUCH in 1 CARTON (85592-829-30) / 20 g in 1 POUCH (85592-829-01)