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
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)
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)
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)
82804-063-30	82804-063	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20240130	N/A	ANDA	ANDA070848	Proficient Rx LP	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE (82804-063-30)
82804-063-60	82804-063	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20240130	N/A	ANDA	ANDA070848	Proficient Rx LP	SUCRALFATE	1 g/1	60 TABLET in 1 BOTTLE (82804-063-60)
82804-063-90	82804-063	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20240130	N/A	ANDA	ANDA070848	Proficient Rx LP	SUCRALFATE	1 g/1	90 TABLET in 1 BOTTLE (82804-063-90)
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)
0615-4517-30	0615-4517	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20100108	20260131	ANDA	ANDA070848	NCS HealthCare of KY, LLC dba Vangard Labs	SUCRALFATE	1 g/1	6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-4517-30) / 5 TABLET in 1 BLISTER PACK
0615-4517-39	0615-4517	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20100108	N/A	ANDA	ANDA070848	NCS HealthCare of KY, LLC dba Vangard Labs	SUCRALFATE	1 g/1	30 TABLET in 1 BLISTER PACK (0615-4517-39)
51655-031-52	51655-031	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20150209	N/A	ANDA	ANDA070848	Northwind Pharmaceuticals, LLC	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE, DISPENSING (51655-031-52)
63629-1307-0	63629-1307	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20221108	N/A	ANDA	ANDA070848	Bryant Ranch Prepack	SUCRALFATE	1 g/1	28 TABLET in 1 BOTTLE (63629-1307-0)
63629-1307-1	63629-1307	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20070205	N/A	ANDA	ANDA070848	Bryant Ranch Prepack	SUCRALFATE	1 g/1	100 TABLET in 1 BOTTLE (63629-1307-1)
63629-1307-2	63629-1307	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20100412	N/A	ANDA	ANDA070848	Bryant Ranch Prepack	SUCRALFATE	1 g/1	60 TABLET in 1 BOTTLE (63629-1307-2)
63629-1307-3	63629-1307	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20080919	N/A	ANDA	ANDA070848	Bryant Ranch Prepack	SUCRALFATE	1 g/1	30 TABLET in 1 BOTTLE (63629-1307-3)
63629-1307-4	63629-1307	HUMAN PRESCRIPTION DRUG	Sucralfate	Sucralfate	TABLET	ORAL	20131017	N/A	ANDA	ANDA070848	Bryant Ranch Prepack	SUCRALFATE	1 g/1	20 TABLET in 1 BOTTLE (63629-1307-4)