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 44 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)
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)
70518-0282-0 70518-0282 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20170303 N/A ANDA ANDA079163 REMEDYREPACK INC. DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-0282-0)
50090-4409-0 50090-4409 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20190715 N/A ANDA ANDA079163 A-S Medication Solutions DIVALPROEX SODIUM 500 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-4409-0)
51655-365-52 51655-365 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20200529 N/A ANDA ANDA079163 Northwind Pharmaceuticals, LLC DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-365-52)
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)
55700-938-60 55700-938 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210910 N/A ANDA ANDA079163 Quality Care Products, LLC DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55700-938-60)
55700-939-60 55700-939 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210910 N/A ANDA ANDA079163 Quality Care Products, LLC DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (55700-939-60)
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)
68001-473-00 68001-473 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-473-00)
68001-473-03 68001-473 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-473-03)
68001-474-00 68001-474 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-474-00)
68001-474-03 68001-474 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20210120 N/A ANDA ANDA079163 BluePoint Laboratories DIVALPROEX SODIUM 500 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-474-03)
63187-742-30 63187-742 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-30)
63187-742-60 63187-742 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-60)
63187-742-90 63187-742 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 250 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-90)
63187-743-30 63187-743 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-30)
63187-743-60 63187-743 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-60)
63187-743-90 63187-743 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20161003 N/A ANDA ANDA079163 Proficient Rx LP DIVALPROEX SODIUM 500 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-743-90)
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