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
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)
70518-3987-1	70518-3987	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20251013	N/A	NDA AUTHORIZED GENERIC	NDA018333	REMEDYREPACK INC.	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-3987-1)
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)
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)
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)
71335-2637-6	71335-2637	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20250602	N/A	NDA AUTHORIZED GENERIC	NDA018333	Bryant Ranch Prepack	SUCRALFATE	1 g/1	150 TABLET in 1 BOTTLE (71335-2637-6)
71335-2637-7	71335-2637	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20250602	N/A	NDA AUTHORIZED GENERIC	NDA018333	Bryant Ranch Prepack	SUCRALFATE	1 g/1	90 TABLET in 1 BOTTLE (71335-2637-7)
71335-2637-8	71335-2637	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20250602	N/A	NDA AUTHORIZED GENERIC	NDA018333	Bryant Ranch Prepack	SUCRALFATE	1 g/1	40 TABLET in 1 BOTTLE (71335-2637-8)
71335-2637-9	71335-2637	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20250602	N/A	NDA AUTHORIZED GENERIC	NDA018333	Bryant Ranch Prepack	SUCRALFATE	1 g/1	120 TABLET in 1 BOTTLE (71335-2637-9)
71335-2637-0	71335-2637	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20250602	N/A	NDA AUTHORIZED GENERIC	NDA018333	Bryant Ranch Prepack	SUCRALFATE	1 g/1	28 TABLET in 1 BOTTLE (71335-2637-0)
71335-2637-1	71335-2637	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20250602	N/A	NDA AUTHORIZED GENERIC	NDA018333	Bryant Ranch Prepack	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE (71335-2637-1)
71335-2637-2	71335-2637	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20250602	N/A	NDA AUTHORIZED GENERIC	NDA018333	Bryant Ranch Prepack	SUCRALFATE	1 g/1	60 TABLET in 1 BOTTLE (71335-2637-2)
71335-2637-3	71335-2637	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20250602	N/A	NDA AUTHORIZED GENERIC	NDA018333	Bryant Ranch Prepack	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE (71335-2637-3)
71335-2637-4	71335-2637	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20250602	N/A	NDA AUTHORIZED GENERIC	NDA018333	Bryant Ranch Prepack	SUCRALFATE	1 g/1	20 TABLET in 1 BOTTLE (71335-2637-4)
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)
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)
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)