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
60687-211-21 60687-211 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20160909 20260228 ANDA ANDA090554 American Health Packaging DIVALPROEX SODIUM 125 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-211-21) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-211-11)
55154-4679-0 55154-4679 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20160126 20260630 ANDA ANDA090554 Cardinal Health 107, LLC DIVALPROEX SODIUM 500 mg/1 10 BLISTER PACK in 1 BAG (55154-4679-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
57237-048-01 57237-048 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Rising Pharma Holdings, Inc. DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-048-01)
57237-048-05 57237-048 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Rising Pharma Holdings, Inc. DIVALPROEX SODIUM 500 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-048-05)
57237-106-05 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/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (57237-106-05)
65862-402-39 65862-402 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 250 mg/1 3000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-39)
65862-402-99 65862-402 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 250 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-99)
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)
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)
55154-7145-0 55154-7145 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20150302 20260630 ANDA ANDA090554 Cardinal Health 107, LLC DIVALPROEX SODIUM 250 mg/1 10 BLISTER PACK in 1 BAG (55154-7145-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
65862-402-01 65862-402 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-01)
65862-402-05 65862-402 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-402-05)
65862-402-10 65862-402 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20141024 N/A ANDA ANDA090554 Aurobindo Pharma Limited DIVALPROEX SODIUM 250 mg/1 10 BLISTER PACK in 1 CARTON (65862-402-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
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)
65862-959-99 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)
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)
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