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 1 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
0904-6860-61 0904-6860 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Major Pharmaceuticals DIVALPROEX SODIUM 250 mg/1 100 BLISTER PACK in 1 CARTON (0904-6860-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
0904-6861-61 0904-6861 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Major Pharmaceuticals DIVALPROEX SODIUM 500 mg/1 100 BLISTER PACK in 1 CARTON (0904-6861-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
0904-6861-90 0904-6861 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20080729 N/A ANDA ANDA078597 Major Pharmaceuticals DIVALPROEX SODIUM 500 mg/1 90 BLISTER PACK in 1 CARTON (0904-6861-90) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
70518-1558-0 70518-1558 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20181019 N/A ANDA ANDA078597 REMEDYREPACK INC. DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-1558-0)
70518-1558-1 70518-1558 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20191016 N/A ANDA ANDA078597 REMEDYREPACK INC. DIVALPROEX SODIUM 500 mg/1 100 POUCH in 1 BOX (70518-1558-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-1558-2)
72789-353-01 72789-353 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20231018 N/A ANDA ANDA078597 PD-Rx Pharmaceuticals, Inc. DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-353-01)
72789-354-01 72789-354 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20231017 N/A ANDA ANDA078597 PD-Rx Pharmaceuticals, Inc. DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-354-01)
71335-2277-1 71335-2277 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20231207 N/A ANDA ANDA078597 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-1)
71335-2277-2 71335-2277 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20231207 N/A ANDA ANDA078597 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-2)
71335-2277-3 71335-2277 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20231207 N/A ANDA ANDA078597 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-3)
71335-2277-4 71335-2277 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20231207 N/A ANDA ANDA078597 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-4)
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)
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)
71335-2344-3 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 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-3)
71335-2344-4 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/1 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-4)
71335-2344-5 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/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2344-5)
70518-2665-0 70518-2665 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20200330 N/A ANDA ANDA078597 REMEDYREPACK INC. DIVALPROEX SODIUM 125 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2665-0)
70518-2665-1 70518-2665 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20231031 N/A ANDA ANDA078597 REMEDYREPACK INC. DIVALPROEX SODIUM 125 mg/1 100 POUCH in 1 BOX (70518-2665-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-2665-2)
70518-2674-2 70518-2674 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210430 N/A ANDA ANDA078597 REMEDYREPACK INC. DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-2674-2)
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
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