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
72578-081-01	72578-081	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230520	N/A	ANDA	ANDA215705	Viona Pharmaceuticals Inc	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE (72578-081-01)
72578-081-05	72578-081	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230520	N/A	ANDA	ANDA215705	Viona Pharmaceuticals Inc	SUCRALFATE	1 g/1	500 TABLET in 1 BOTTLE (72578-081-05)
70518-3959-0	70518-3959	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20231213	N/A	ANDA	ANDA215705	REMEDYREPACK INC.	SUCRALFATE	1 g/1	30 TABLET in 1 BLISTER PACK (70518-3959-0)
72578-081-06	72578-081	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230520	N/A	ANDA	ANDA215705	Viona Pharmaceuticals Inc	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE (72578-081-06)
70771-1833-5	70771-1833	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230520	N/A	ANDA	ANDA215705	Zydus Lifesciences Limited	SUCRALFATE	1 g/1	500 TABLET in 1 BOTTLE (70771-1833-5)
70771-1833-3	70771-1833	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230520	N/A	ANDA	ANDA215705	Zydus Lifesciences Limited	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE (70771-1833-3)
70771-1833-1	70771-1833	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230520	N/A	ANDA	ANDA215705	Zydus Lifesciences Limited	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE (70771-1833-1)