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)
检索条件:" 注册申请号=ANDA070848"
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)
55154-4379-0 55154-4379 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20130924 N/A ANDA ANDA070848 Cardinal Health 107, LLC SUCRALFATE 1 g/1 10 BLISTER PACK in 1 BAG (55154-4379-0) / 1 TABLET in 1 BLISTER PACK
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)
51079-753-20 51079-753 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20130924 N/A ANDA ANDA070848 Mylan Institutional Inc. SUCRALFATE 1 g/1 100 BLISTER PACK in 1 CARTON (51079-753-20) / 1 TABLET in 1 BLISTER PACK (51079-753-01)
0615-4517-30 0615-4517 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20100108 N/A ANDA ANDA070848 NCS HealthCare of KY, Inc 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, Inc dba Vangard Labs SUCRALFATE 1 g/1 30 TABLET in 1 BLISTER PACK (0615-4517-39)
50090-0582-0 50090-0582 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20141128 N/A ANDA ANDA070848 A-S Medication Solutions SUCRALFATE 1 g/1 60 TABLET in 1 BOTTLE (50090-0582-0)
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)
80425-0091-1 80425-0091 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 19961111 N/A ANDA ANDA070848 Advanced Rx Pharmacy of Tennessee, LLC SUCRALFATE 1 g/1 30 TABLET in 1 BOTTLE (80425-0091-1)
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)
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)
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)
63739-943-10 63739-943 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20160314 N/A ANDA ANDA070848 McKesson Corporation dba SKY Packaging SUCRALFATE 1 g/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-943-10) / 10 TABLET in 1 BLISTER PACK
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