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
58914-171-10	58914-171	HUMAN PRESCRIPTION DRUG	Carafate	Sucralfate	TABLET	ORAL	19811030	N/A	NDA	NDA018333	Allergan, Inc.	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE (58914-171-10)
51655-475-52	51655-475	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20201118	N/A	NDA AUTHORIZED GENERIC	NDA018333	Northwind Pharmaceuticals, LLC	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-475-52)
80425-0213-1	80425-0213	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230103	N/A	NDA AUTHORIZED GENERIC	NDA018333	Advanced Rx Pharmacy of Tennessee, LLC	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE (80425-0213-1)
71610-017-60	71610-017	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20171227	N/A	NDA AUTHORIZED GENERIC	NDA018333	Aphena Pharma Solutions - Tennessee, LLC	SUCRALFATE	1 g/1	90 TABLET in 1 BOTTLE (71610-017-60)
71610-017-70	71610-017	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20180119	N/A	NDA AUTHORIZED GENERIC	NDA018333	Aphena Pharma Solutions - Tennessee, LLC	SUCRALFATE	1 g/1	120 TABLET in 1 BOTTLE (71610-017-70)
71610-017-94	71610-017	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20180119	N/A	NDA AUTHORIZED GENERIC	NDA018333	Aphena Pharma Solutions - Tennessee, LLC	SUCRALFATE	1 g/1	360 TABLET in 1 BOTTLE (71610-017-94)
67296-2090-4	67296-2090	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20170925	N/A	NDA AUTHORIZED GENERIC	NDA018333	Redpharm drug	SUCRALFATE	1 g/1	40 TABLET in 1 BOTTLE (67296-2090-4)
70518-3987-0	70518-3987	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20240118	N/A	NDA AUTHORIZED GENERIC	NDA018333	REMEDYREPACK INC.	SUCRALFATE	1 g/1	30 TABLET in 1 BLISTER PACK (70518-3987-0)
68788-8316-1	68788-8316	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20221223	N/A	NDA AUTHORIZED GENERIC	NDA018333	Preferred Pharmaceuticals Inc.	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE (68788-8316-1)
68788-8316-3	68788-8316	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20221223	N/A	NDA AUTHORIZED GENERIC	NDA018333	Preferred Pharmaceuticals Inc.	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE (68788-8316-3)
80425-0377-1	80425-0377	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20230313	N/A	NDA AUTHORIZED GENERIC	NDA018333	Advanced Rx Pharmacy of Tennessee, LLC	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE (80425-0377-1)
50090-5287-0	50090-5287	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20201022	N/A	NDA AUTHORIZED GENERIC	NDA018333	A-S Medication Solutions	SUCRALFATE	1 g/1	60 TABLET in 1 BOTTLE (50090-5287-0)
59762-0401-1	59762-0401	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20170925	N/A	NDA AUTHORIZED GENERIC	NDA018333	Greenstone LLC	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE (59762-0401-1)
59762-0401-5	59762-0401	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20170925	N/A	NDA AUTHORIZED GENERIC	NDA018333	Greenstone LLC	SUCRALFATE	1 g/1	500 TABLET in 1 BOTTLE (59762-0401-5)