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"
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
70518-1298-6 70518-1298 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220605 N/A ANDA ANDA202038 REMEDYREPACK INC. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1298-6)
70518-1298-8 70518-1298 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20240926 N/A ANDA ANDA202038 REMEDYREPACK INC. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-1298-8)
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)
60760-646-30 60760-646 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220825 N/A ANDA ANDA202038 ST. MARY'S MEDICAL PARK PHARMACY PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-646-30)
83008-034-30 83008-034 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230718 20270131 ANDA ANDA202038 Quality Care Products, LLC PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (83008-034-30)
83008-034-60 83008-034 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230718 20270331 ANDA ANDA202038 Quality Care Products, LLC PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (83008-034-60)
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)
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)
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)
60760-639-60 60760-639 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20220622 N/A ANDA ANDA202038 St Mary's Medical Park Pharmacy PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-639-60)
55154-4165-0 55154-4165 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20120928 N/A ANDA ANDA202038 Cardinal Health 107, LLC PANTOPRAZOLE SODIUM 40 mg/1 10 BLISTER PACK in 1 BAG (55154-4165-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
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