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=ANDA078597"
符合检索条件的记录共 42 条，共 3 页，当前第 2 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
71335-2344-1 71335-2344 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20240206 N/A ANDA ANDA078597 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-1)
70518-3431-0 70518-3431 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220603 N/A ANDA ANDA078597 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3431-0)
70518-3431-1 70518-3431 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220603 N/A ANDA ANDA078597 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3431-1)
70518-3431-2 70518-3431 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220628 N/A ANDA ANDA078597 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 100 POUCH in 1 BOX (70518-3431-2) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3431-3)
71335-2344-2 71335-2344 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20240206 N/A ANDA ANDA078597 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-2)
70518-2513-0 70518-2513 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20191230 N/A ANDA ANDA078597 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 100 POUCH in 1 BOX (70518-2513-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2513-1)
55154-4154-0 55154-4154 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Cardinal Health 107, LLC DIVALPROEX SODIUM 250 mg/1 10 BLISTER PACK in 1 BAG (55154-4154-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
62756-796-18 62756-796 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 125 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-18)
62756-796-88 62756-796 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 125 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-88)
62756-797-08 62756-797 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-08)
62756-797-13 62756-797 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-13)
62756-797-18 62756-797 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 250 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-18)
62756-797-83 62756-797 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-83)
62756-797-88 62756-797 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-797-88)
62756-798-08 62756-798 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-08)
62756-798-13 62756-798 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 500 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-13)
62756-798-18 62756-798 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 500 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-18)
62756-798-83 62756-798 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-83)
62756-798-88 62756-798 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-798-88)
62756-796-83 62756-796 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Sun Pharmaceutical Industries, Inc. DIVALPROEX SODIUM 125 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (62756-796-83)
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