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
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)
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)
48433-091-20 48433-091 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20260313 N/A ANDA ANDA070848 Safecor Health LLC SUCRALFATE 1 g/1 100 BLISTER PACK in 1 CARTON (48433-091-20) / 1 TABLET in 1 BLISTER PACK (48433-091-01)
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)
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)
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)
0615-4517-39 0615-4517 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20100108 20261130 ANDA ANDA070848 NCS HealthCare of KY, LLC dba Vangard Labs SUCRALFATE 1 g/1 30 TABLET in 1 BLISTER PACK (0615-4517-39)
87063-176-01 87063-176 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20260518 N/A ANDA ANDA070848 ASCLEMED USA INC. SUCRALFATE 1 g/1 100 TABLET in 1 BOTTLE (87063-176-01)
87063-176-05 87063-176 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20260518 N/A ANDA ANDA070848 ASCLEMED USA INC. SUCRALFATE 1 g/1 500 TABLET in 1 BOTTLE (87063-176-05)
87063-176-12 87063-176 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20260518 N/A ANDA ANDA070848 ASCLEMED USA INC. SUCRALFATE 1 g/1 120 TABLET in 1 BOTTLE (87063-176-12)
87063-176-30 87063-176 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20260518 N/A ANDA ANDA070848 ASCLEMED USA INC. SUCRALFATE 1 g/1 30 TABLET in 1 BOTTLE (87063-176-30)
87063-176-60 87063-176 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20260518 N/A ANDA ANDA070848 ASCLEMED USA INC. SUCRALFATE 1 g/1 60 TABLET in 1 BOTTLE (87063-176-60)
87063-176-90 87063-176 HUMAN PRESCRIPTION DRUG Sucralfate Sucralfate TABLET ORAL 20260518 N/A ANDA ANDA070848 ASCLEMED USA INC. SUCRALFATE 1 g/1 90 TABLET in 1 BOTTLE (87063-176-90)
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)
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)
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