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 4 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
80425-0162-1 80425-0162 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-1)
80425-0162-2 80425-0162 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-2)
80425-0162-3 80425-0162 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0162-3)
67046-0155-3 67046-0155 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20241106 N/A ANDA ANDA202882 Coupler LLC PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (67046-0155-3)
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)
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)
76420-668-90 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 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-668-90)
80425-0133-1 80425-0133 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0133-1)
80425-0133-2 80425-0133 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0133-2)
80425-0133-3 80425-0133 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0133-3)
72189-112-30 72189-112 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM pantoprazole TABLET, DELAYED RELEASE ORAL 20200612 N/A ANDA ANDA202882 DIRECT RX PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-30)
63187-654-90 63187-654 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20181201 N/A ANDA ANDA202882 Proficient Rx LP PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-654-90)
72865-229-90 72865-229 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220501 N/A ANDA ANDA202882 XLCare Pharmaceuticals Inc. PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72865-229-90)
76420-671-01 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-01)
76420-671-10 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-10)
76420-671-30 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-30)
76420-671-60 76420-671 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-671-60)
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