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=ANDA208644"
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
60760-560-07 60760-560 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20241030 N/A ANDA ANDA208644 St. Mary's Medical Park Pharmacy RABEPRAZOLE SODIUM 20 mg/1 7 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-560-07)
60760-560-30 60760-560 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20190910 N/A ANDA ANDA208644 St. Mary's Medical Park Pharmacy RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-560-30)
60760-560-60 60760-560 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20251104 N/A ANDA ANDA208644 St. Mary's Medical Park Pharmacy RABEPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-560-60)
71205-292-30 71205-292 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20190701 N/A ANDA ANDA208644 Proficient Rx LP RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-292-30)
71205-292-60 71205-292 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20190701 N/A ANDA ANDA208644 Proficient Rx LP RABEPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-292-60)
71205-292-90 71205-292 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20190701 N/A ANDA ANDA208644 Proficient Rx LP RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-292-90)
72189-169-30 72189-169 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE ORAL 20210114 N/A ANDA ANDA208644 DIRECT RX RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-30)
72189-169-60 72189-169 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE ORAL 20210114 N/A ANDA ANDA208644 DIRECT RX RABEPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-60)
72189-169-90 72189-169 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM RABEPRAZOLE SODIUM TABLET, DELAYED RELEASE ORAL 20210114 N/A ANDA ANDA208644 DIRECT RX RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-169-90)
55700-767-30 55700-767 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20190621 20260131 ANDA ANDA208644 Quality Care Products, LLC RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-767-30)
72162-2367-5 72162-2367 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20240716 N/A ANDA ANDA208644 Bryant Ranch Prepack RABEPRAZOLE SODIUM 20 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2367-5)
50090-4751-0 50090-4751 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20191125 N/A ANDA ANDA208644 A-S Medication Solutions RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-0)
50090-4751-1 50090-4751 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20191125 N/A ANDA ANDA208644 A-S Medication Solutions RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4751-1)
67877-443-30 67877-443 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20180427 N/A ANDA ANDA208644 Ascend Laboratories, LLC RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-443-30)
67877-443-38 67877-443 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20180427 N/A ANDA ANDA208644 Ascend Laboratories, LLC RABEPRAZOLE SODIUM 20 mg/1 100 POUCH in 1 CARTON (67877-443-38) / 1 BLISTER PACK in 1 POUCH / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67877-443-33)
67877-443-90 67877-443 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20180427 N/A ANDA ANDA208644 Ascend Laboratories, LLC RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (67877-443-90)
80425-0094-1 80425-0094 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium DR Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20180427 N/A ANDA ANDA208644 Advanced Rx of Tennessee, LLC RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0094-1)
80425-0094-2 80425-0094 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium DR Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20180427 N/A ANDA ANDA208644 Advanced Rx of Tennessee, LLC RABEPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0094-2)
70518-2590-0 70518-2590 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20200218 N/A ANDA ANDA208644 REMEDYREPACK INC. RABEPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-2590-0)
76420-818-30 76420-818 HUMAN PRESCRIPTION DRUG Rabeprazole Sodium Rabeprazole Sodium TABLET, DELAYED RELEASE ORAL 20240625 N/A ANDA ANDA208644 Asclemed USA, Inc. RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-818-30)
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