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=ANDA090554"
符合检索条件的记录共 41 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
65862-403-01 65862-403 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-01)
65862-403-05 65862-403 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 500 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-05)
70518-3683-0 70518-3683 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230317 N/A ANDA ANDA090554 REMEDYREPACK INC. DIVALPROEX SODIUM 125 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3683-0)
70518-3683-1 70518-3683 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230913 N/A ANDA ANDA090554 REMEDYREPACK INC. DIVALPROEX SODIUM 125 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3683-1)
70518-3683-2 70518-3683 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250701 N/A ANDA ANDA090554 REMEDYREPACK INC. DIVALPROEX SODIUM 125 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3683-2)
50090-7121-0 50090-7121 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20240327 N/A ANDA ANDA090554 A-S Medication Solutions DIVALPROEX SODIUM 125 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-7121-0)
57237-047-01 57237-047 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Rising Pharma Holdings, Inc. DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-047-01)
57237-047-05 57237-047 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Rising Pharma Holdings, Inc. DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-047-05)
70518-3055-3 70518-3055 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220809 N/A ANDA ANDA090554 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 100 POUCH in 1 BOX (70518-3055-3) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3055-4)
70518-3055-5 70518-3055 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230104 N/A ANDA ANDA090554 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3055-5)
70518-3055-6 70518-3055 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230501 N/A ANDA ANDA090554 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3055-6)
70518-3055-7 70518-3055 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250630 N/A ANDA ANDA090554 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (70518-3055-7)
65862-403-10 65862-403 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 500 mg/1 10 BLISTER PACK in 1 CARTON (65862-403-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
65862-403-22 65862-403 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 500 mg/1 2000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-403-22)
57237-106-01 57237-106 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Rising Pharma Holdings, Inc. DIVALPROEX SODIUM 125 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-106-01)
65862-959-01 65862-959 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 125 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-01)
65862-959-05 65862-959 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 125 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-05)
65862-959-10 65862-959 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 125 mg/1 10 BLISTER PACK in 1 CARTON (65862-959-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
65862-959-71 65862-959 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 125 mg/1 7000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-71)
65862-959-99 65862-959 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 125 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-959-99)
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