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
0093-2210-01	0093-2210	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	19961111	N/A	ANDA	ANDA070848	Teva Pharmaceuticals USA, Inc.	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE (0093-2210-01)
0093-2210-05	0093-2210	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	19961111	N/A	ANDA	ANDA070848	Teva Pharmaceuticals USA, Inc.	SUCRALFATE	1 g/1	500 TABLET in 1 BOTTLE (0093-2210-05)
0093-2210-98	0093-2210	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20110112	N/A	ANDA	ANDA070848	Teva Pharmaceuticals USA, Inc.	SUCRALFATE	1 g/1	90 TABLET in 1 BOTTLE (0093-2210-98)
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)
70518-0775-0	70518-0775	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20171010	N/A	ANDA	ANDA070848	REMEDYREPACK INC.	SUCRALFATE	1 g/1	30 TABLET in 1 BLISTER PACK (70518-0775-0)
70518-0775-2	70518-0775	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20210218	N/A	ANDA	ANDA070848	REMEDYREPACK INC.	SUCRALFATE	1 g/1	30 TABLET in 1 BLISTER PACK (70518-0775-2)