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=ANDA204237"
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
50090-6887-1 50090-6887 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20231206 N/A ANDA ANDA204237 A-S Medication Solutions RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-6887-1)
80425-0363-3 80425-0363 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20231023 N/A ANDA ANDA204237 Advanced Rx of Tennessee, LLC RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0363-3)
72162-2503-5 72162-2503 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20170601 N/A ANDA ANDA204237 Bryant Ranch Prepack RABEPRAZOLE SODIUM 20 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2503-5)
72162-2503-9 72162-2503 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20170601 N/A ANDA ANDA204237 Bryant Ranch Prepack RABEPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2503-9)
72162-2503-3 72162-2503 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20170601 N/A ANDA ANDA204237 Bryant Ranch Prepack RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2503-3)
80425-0363-1 80425-0363 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20231023 N/A ANDA ANDA204237 Advanced Rx of Tennessee, LLC RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0363-1)
80425-0363-2 80425-0363 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20231023 N/A ANDA ANDA204237 Advanced Rx of Tennessee, LLC RABEPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0363-2)
60760-972-07 60760-972 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20240319 N/A ANDA ANDA204237 St. Mary's Medical Park Pharmacy RABEPRAZOLE SODIUM 20 mg/1 7 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-972-07)
60760-972-30 60760-972 HUMAN PRESCRIPTION DRUG RABEPRAZOLE SODIUM rabeprazole sodium TABLET, DELAYED RELEASE ORAL 20210506 N/A ANDA ANDA204237 St. Mary's Medical Park Pharmacy RABEPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-972-30)
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