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 93 条，共 5 页，当前第 3 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
80425-0133-1 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)
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)
76420-669-30 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-30)
76420-669-60 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-60)
72789-268-30 72789-268 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20220812 N/A ANDA ANDA202882 PD-Rx Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-268-30)
68071-2285-6 68071-2285 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20201027 N/A ANDA ANDA202882 NuCare Pharmaceuticals,Inc. PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-2285-6)
80425-0278-1 80425-0278 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230330 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0278-1)
80425-0278-2 80425-0278 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230228 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0278-2)
80425-0278-3 80425-0278 HUMAN PRESCRIPTION DRUG Pantoprazole Sodium DR Pantoprazole Sodium TABLET, DELAYED RELEASE ORAL 20230228 N/A ANDA ANDA202882 Advanced Rx Pharmacy of Tennessee, LLC PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0278-3)
76420-669-90 76420-669 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240214 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-90)
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)
31722-712-90 31722-712 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Camber Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-712-90)
31722-713-31 31722-713 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Camber Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 40 mg/1 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (31722-713-31)
31722-713-32 31722-713 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Camber Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 40 mg/1 10 TABLET, DELAYED RELEASE in 1 CARTON (31722-713-32)
31722-713-90 31722-713 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Camber Pharmaceuticals, Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (31722-713-90)
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