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 47 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
29300-140-05 29300-140 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20111001 N/A ANDA ANDA079163 Unichem Pharmaceuticals (USA), Inc. DIVALPROEX SODIUM 500 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-05)
29300-140-10 29300-140 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20111001 N/A ANDA ANDA079163 Unichem Pharmaceuticals (USA), Inc. DIVALPROEX SODIUM 500 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-10)
70518-3620-0 70518-3620 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230121 N/A ANDA ANDA079163 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 100 POUCH in 1 BOX (70518-3620-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3620-1)
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)
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)
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)
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)
50090-4861-0 50090-4861 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20200122 N/A ANDA ANDA079163 A-S Medication Solutions DIVALPROEX SODIUM 125 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4861-0)
71335-0008-1 71335-0008 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20181221 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-1)
71335-0008-2 71335-0008 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20180306 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-2)
71335-0008-3 71335-0008 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20180301 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-3)
71335-0008-4 71335-0008 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20211227 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-4)
71335-2862-1 71335-2862 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20251023 N/A ANDA ANDA079163 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2862-1)
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