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
55154-4379-0	55154-4379	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20130924	N/A	ANDA	ANDA070848	Cardinal Health 107, LLC	SUCRALFATE	1 g/1	10 BLISTER PACK in 1 BAG (55154-4379-0) / 1 TABLET in 1 BLISTER PACK
68071-1749-1	68071-1749	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20200424	N/A	ANDA	ANDA070848	NuCare Pharmaceuticals,Inc.	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE (68071-1749-1)
80425-0091-1	80425-0091	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	19961111	N/A	ANDA	ANDA070848	Advanced Rx of Tennessee, LLC	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE (80425-0091-1)
68788-8946-1	68788-8946	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20151028	N/A	ANDA	ANDA070848	Preferred Pharmaceuticals Inc.	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE (68788-8946-1)
68788-8946-3	68788-8946	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20151028	N/A	ANDA	ANDA070848	Preferred Pharmaceuticals Inc.	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE (68788-8946-3)
51079-753-20	51079-753	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20130924	N/A	ANDA	ANDA070848	Mylan Institutional Inc.	SUCRALFATE	1 g/1	100 BLISTER PACK in 1 CARTON (51079-753-20) / 1 TABLET in 1 BLISTER PACK (51079-753-01)
72189-234-20	72189-234	HUMAN PRESCRIPTION DRUG	SUCRALFATE	SUCRALFATE	TABLET	ORAL	20210618	N/A	ANDA	ANDA070848	DIRECT RX	SUCRALFATE	1 g/1	20 TABLET in 1 BOTTLE (72189-234-20)
72189-234-90	72189-234	HUMAN PRESCRIPTION DRUG	SUCRALFATE	SUCRALFATE	TABLET	ORAL	20210618	N/A	ANDA	ANDA070848	DIRECT RX	SUCRALFATE	1 g/1	90 TABLET in 1 BOTTLE (72189-234-90)