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"
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
65862-402-01 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
65862-402-39 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)
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)
68084-782-61 68084-782 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20160126 20260630 ANDA ANDA090554 American Health Packaging DIVALPROEX SODIUM 500 mg/1 90 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-782-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-782-11)
60760-698-60 60760-698 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20250513 N/A ANDA ANDA090554 ST. MARY'S MEDICAL PARK PHARMACY DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-698-60)
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)
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)
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)
68084-776-01 68084-776 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20150302 20260630 ANDA ANDA090554 American Health Packaging DIVALPROEX SODIUM 250 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-776-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (68084-776-11)
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)
71335-2158-1 71335-2158 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220811 N/A ANDA ANDA090554 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-1)
71335-2158-2 71335-2158 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230302 N/A ANDA ANDA090554 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-2)
71335-2158-3 71335-2158 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220811 N/A ANDA ANDA090554 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-3)
71335-2158-4 71335-2158 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20240906 N/A ANDA ANDA090554 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 180 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2158-4)
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