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=ANDA079163"
符合检索条件的记录共 51 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
50090-2007-0 50090-2007 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20150918 N/A ANDA ANDA079163 A-S Medication Solutions DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-2007-0)
71335-2124-1 71335-2124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220719 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-1)
71335-2124-2 71335-2124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220719 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-2)
71335-2124-3 71335-2124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220719 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-3)
71335-2124-4 71335-2124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220719 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-4)
50090-2007-1 50090-2007 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20170802 N/A ANDA ANDA079163 A-S Medication Solutions DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-2007-1)
68001-472-00 68001-472 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 125 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-00)
68001-472-03 68001-472 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 125 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-03)
63629-4278-1 63629-4278 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20211222 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-1)
63629-4278-2 63629-4278 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20121119 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-2)
63629-4278-3 63629-4278 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141110 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-3)
63629-4278-4 63629-4278 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20180531 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 180 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-4)
63629-4278-5 63629-4278 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20180917 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-5)
60687-879-61 60687-879 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250206 N/A ANDA ANDA079163 American Health Packaging DIVALPROEX SODIUM 500 mg/1 90 BLISTER PACK in 1 CARTON (60687-879-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-879-11)
70518-4575-0 70518-4575 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20260217 N/A ANDA ANDA079163 REMEDYREPACK INC. DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-4575-0)
72162-2460-1 72162-2460 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250221 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-1)
72162-2460-3 72162-2460 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250221 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-3)
61919-249-30 61919-249 HUMAN PRESCRIPTION DRUG DIVALPROEX SODIUM divalproex sodium TABLET, DELAYED RELEASE ORAL 20220406 N/A ANDA ANDA079163 DirectRx DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-30)
61919-249-60 61919-249 HUMAN PRESCRIPTION DRUG DIVALPROEX SODIUM divalproex sodium TABLET, DELAYED RELEASE ORAL 20220406 N/A ANDA ANDA079163 DirectRx DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-60)
60687-857-21 60687-857 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250317 N/A ANDA ANDA079163 American Health Packaging DIVALPROEX SODIUM 125 mg/1 30 BLISTER PACK in 1 CARTON (60687-857-21) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-857-11)
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