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 50 条，共 3 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
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)
68071-3553-6 68071-3553 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20231207 N/A ANDA ANDA078597 NuCare Pharmaceuticals,Inc. DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3553-6)
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
60760-798-60 60760-798 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250513 N/A ANDA ANDA078597 ST. MARY'S MEDICAL PARK PHARMACY DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-798-60)
71335-2277-1 71335-2277 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20231129 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 20240530 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 20240530 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 20240530 N/A ANDA ANDA078597 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2277-4)
72162-2316-1 72162-2316 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20240516 N/A ANDA ANDA078597 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-1)
72162-2316-5 72162-2316 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20240516 N/A ANDA ANDA078597 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2316-5)
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)
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)
62756-798-88 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)
72189-636-60 72189-636 HUMAN PRESCRIPTION DRUG Divalproex Sodium D/R Divalproex Sodium D/R TABLET, DELAYED RELEASE ORAL 20250728 N/A ANDA ANDA078597 Direct_Rx DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (72189-636-60)
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)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase