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
72162-2264-5	72162-2264	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20240223	N/A	ANDA	ANDA074415	Bryant Ranch Prepack	SUCRALFATE	1 g/1	500 TABLET in 1 BOTTLE, PLASTIC (72162-2264-5)
68071-3478-3	68071-3478	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230803	N/A	ANDA	ANDA074415	NuCare Pharmaceuticals,Inc.	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE, PLASTIC (68071-3478-3)
82804-102-30	82804-102	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20240506	N/A	ANDA	ANDA074415	Proficient Rx LP	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE, PLASTIC (82804-102-30)
63629-9152-1	63629-9152	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20220126	N/A	ANDA	ANDA074415	Bryant Ranch Prepack	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE, PLASTIC (63629-9152-1)
72189-429-20	72189-429	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230302	N/A	ANDA	ANDA074415	Direct_Rx	SUCRALFATE	1 g/1	20 TABLET in 1 BOTTLE (72189-429-20)
72189-429-90	72189-429	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230302	N/A	ANDA	ANDA074415	Direct_Rx	SUCRALFATE	1 g/1	90 TABLET in 1 BOTTLE (72189-429-90)