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=ANDA202882"
符合检索条件的记录共 112 条，共 6 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
50090-5794-0 50090-5794 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20211011 N/A ANDA ANDA202882 A-S Medication Solutions PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-0)
50090-5794-1 50090-5794 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20211011 N/A ANDA ANDA202882 A-S Medication Solutions PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-5794-1)
45865-263-30 45865-263 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20230815 N/A ANDA ANDA202882 Medsource Pharmaceuticals PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (45865-263-30)
55700-790-30 55700-790 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20190913 N/A ANDA ANDA202882 Quality Care Products, LLC PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-790-30)
55700-790-60 55700-790 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20190913 N/A ANDA ANDA202882 Quality Care Products, LLC PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (55700-790-60)
72189-514-90 72189-514 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium DR TABLET, DELAYED RELEASE ORAL 20230911 N/A ANDA ANDA202882 Direct_Rx PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-514-90)
76420-668-10 76420-668 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-10)
76420-668-30 76420-668 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-30)
76420-668-60 76420-668 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-60)
68071-2215-3 68071-2215 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200708 N/A ANDA ANDA202882 NuCare Pharmaceuticals,Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2215-3)
68071-2215-4 68071-2215 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200708 N/A ANDA ANDA202882 NuCare Pharmaceuticals,Inc. PANTOPRAZOLE SODIUM 40 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2215-4)
53002-1700-3 53002-1700 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20230101 N/A ANDA ANDA202882 RPK Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (53002-1700-3)
53002-1700-9 53002-1700 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20230101 N/A ANDA ANDA202882 RPK Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 3 TABLET, DELAYED RELEASE in 1 BOTTLE (53002-1700-9)
71610-659-09 71610-659 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220825 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 20 mg/1 9000 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-659-09)
71610-659-42 71610-659 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20230217 N/A ANDA ANDA202882 Aphena Pharma Solutions - Tennessee, LLC PANTOPRAZOLE SODIUM 20 mg/1 1800 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-659-42)
72865-230-10 72865-230 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220501 N/A ANDA ANDA202882 XLCare Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-10)
72865-230-90 72865-230 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220501 N/A ANDA ANDA202882 XLCare Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-230-90)
53002-2419-3 53002-2419 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220101 N/A ANDA ANDA202882 RPK Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (53002-2419-3)
53002-2419-5 53002-2419 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220101 N/A ANDA ANDA202882 RPK Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 40 mg/1 15 TABLET, DELAYED RELEASE in 1 BOTTLE (53002-2419-5)
71335-1572-3 71335-1572 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200421 N/A ANDA ANDA202882 Bryant Ranch Prepack PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1572-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase