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 5 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
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)
60760-712-30 60760-712 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200304 N/A ANDA ANDA202882 St. Mary's Medical Park Pharmacy PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-712-30)
60760-712-60 60760-712 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20200304 N/A ANDA ANDA202882 St. Mary's Medical Park Pharmacy PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-712-60)
76420-674-01 76420-674 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-01)
68645-596-54 68645-596 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20140910 N/A ANDA ANDA202882 Legacy Pharmaceutical Packaging, LLC PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68645-596-54)
31722-712-31 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 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK (31722-712-31)
31722-712-32 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 10 TABLET, DELAYED RELEASE in 1 CARTON (31722-712-32)
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)
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)
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)
72189-112-60 72189-112 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM pantoprazole TABLET, DELAYED RELEASE ORAL 20200612 N/A ANDA ANDA202882 DIRECT RX PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-60)
72189-112-90 72189-112 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM pantoprazole TABLET, DELAYED RELEASE ORAL 20200612 N/A ANDA ANDA202882 DIRECT RX PANTOPRAZOLE SODIUM 20 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-112-90)
76420-674-10 76420-674 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-10)
76420-674-30 76420-674 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-30)
76420-674-60 76420-674 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-60)
76420-674-90 76420-674 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20240313 N/A ANDA ANDA202882 Asclemed USA, Inc. PANTOPRAZOLE SODIUM 40 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-674-90)
63187-831-30 63187-831 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20170403 N/A ANDA ANDA202882 Proficient Rx LP PANTOPRAZOLE SODIUM 20 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-30)
63187-831-60 63187-831 HUMAN PRESCRIPTION DRUG PANTOPRAZOLE SODIUM PANTOPRAZOLE TABLET, DELAYED RELEASE ORAL 20170403 N/A ANDA ANDA202882 Proficient Rx LP PANTOPRAZOLE SODIUM 20 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-60)
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