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=ANDA202038"
符合检索条件的记录共 72 条，共 4 页，当前第 2 页 ，可点击列名称排序
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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
65862-559-99 65862-559 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20120928 N/A ANDA ANDA202038 Aurobindo Pharma Limited PANTOPRAZOLE SODIUM 20 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-559-99)
65862-560-05 65862-560 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20251204 N/A ANDA ANDA202038 Aurobindo Pharma Limited PANTOPRAZOLE SODIUM 40 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-560-05)
65862-560-10 65862-560 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20120928 N/A ANDA ANDA202038 Aurobindo Pharma Limited PANTOPRAZOLE SODIUM 40 mg/1 10 BLISTER PACK in 1 CARTON (65862-560-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
65862-560-90 65862-560 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20120928 N/A ANDA ANDA202038 Aurobindo Pharma Limited PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-560-90)
65862-560-99 65862-560 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20120928 N/A ANDA ANDA202038 Aurobindo Pharma Limited PANTOPRAZOLE SODIUM 40 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-560-99)
42708-185-30 42708-185 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20240112 N/A ANDA ANDA202038 QPharma Inc PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-185-30)
60687-725-01 60687-725 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230705 N/A ANDA ANDA202038 American Health Packaging PANTOPRAZOLE SODIUM 20 mg/1 100 BLISTER PACK in 1 CARTON (60687-725-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-725-11)
51655-075-25 51655-075 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20240223 N/A ANDA ANDA202038 Northwind Health Company, LLC PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-075-25)
51655-075-52 51655-075 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220927 N/A ANDA ANDA202038 Northwind Health Company, LLC PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-075-52)
60687-736-01 60687-736 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230705 N/A ANDA ANDA202038 American Health Packaging PANTOPRAZOLE SODIUM 40 mg/1 100 BLISTER PACK in 1 CARTON (60687-736-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-736-11)
60687-736-09 60687-736 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230705 N/A ANDA ANDA202038 American Health Packaging PANTOPRAZOLE SODIUM 40 mg/1 80 BLISTER PACK in 1 CARTON (60687-736-09) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-736-11)
60687-736-65 60687-736 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230705 N/A ANDA ANDA202038 American Health Packaging PANTOPRAZOLE SODIUM 40 mg/1 50 BLISTER PACK in 1 CARTON (60687-736-65) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-736-11)
0615-8113-05 0615-8113 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20221215 N/A ANDA ANDA202038 NCS HealthCare of KY, LLC dba Vangard Labs PANTOPRAZOLE SODIUM 20 mg/1 15 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8113-05)
0615-8113-39 0615-8113 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20181107 N/A ANDA ANDA202038 NCS HealthCare of KY, LLC dba Vangard Labs PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8113-39)
50090-5361-0 50090-5361 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201113 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-0)
50090-5361-1 50090-5361 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201113 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-1)
50090-5361-2 50090-5361 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201113 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5361-2)
50090-5378-0 50090-5378 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201119 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5378-0)
50090-5378-1 50090-5378 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201119 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5378-1)
50090-5379-0 50090-5379 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20201119 N/A ANDA ANDA202038 A-S Medication Solutions PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5379-0)
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