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=ANDA202419"
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
63629-4698-3 63629-4698 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140609 N/A ANDA ANDA202419 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4698-3)
63629-4698-4 63629-4698 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140609 N/A ANDA ANDA202419 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-4698-4)
65862-594-01 65862-594 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 Aurobindo Pharma Limited DIVALPROEX SODIUM 250 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-01)
65862-594-99 65862-594 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 Aurobindo Pharma Limited DIVALPROEX SODIUM 250 mg/1 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-99)
65862-595-01 65862-595 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 Aurobindo Pharma Limited DIVALPROEX SODIUM 500 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-595-01)
65862-595-05 65862-595 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 Aurobindo Pharma Limited DIVALPROEX SODIUM 500 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-595-05)
65862-595-10 65862-595 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 Aurobindo Pharma Limited DIVALPROEX SODIUM 500 mg/1 10 BLISTER PACK in 1 CARTON (65862-595-10) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
50090-4737-0 50090-4737 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191120 N/A ANDA ANDA202419 A-S Medication Solutions DIVALPROEX SODIUM 500 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4737-0)
50090-4737-1 50090-4737 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20191120 N/A ANDA ANDA202419 A-S Medication Solutions DIVALPROEX SODIUM 500 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4737-1)
65862-594-05 65862-594 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 Aurobindo Pharma Limited DIVALPROEX SODIUM 250 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-05)
65862-594-10 65862-594 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 Aurobindo Pharma Limited DIVALPROEX SODIUM 250 mg/1 10 BLISTER PACK in 1 CARTON (65862-594-10) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
65862-594-60 65862-594 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 Aurobindo Pharma Limited DIVALPROEX SODIUM 250 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-60)
16714-484-01 16714-484 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 NorthStar Rx LLC DIVALPROEX SODIUM 250 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-484-01)
16714-484-02 16714-484 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 NorthStar Rx LLC DIVALPROEX SODIUM 250 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-484-02)
16714-485-01 16714-485 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 NorthStar Rx LLC DIVALPROEX SODIUM 500 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-485-01)
16714-485-02 16714-485 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20140602 N/A ANDA ANDA202419 NorthStar Rx LLC DIVALPROEX SODIUM 500 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-485-02)
72162-2515-1 72162-2515 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250609 N/A ANDA ANDA202419 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2515-1)
72162-2516-1 72162-2516 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250609 N/A ANDA ANDA202419 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2516-1)
72162-2516-5 72162-2516 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250609 N/A ANDA ANDA202419 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2516-5)
50090-6074-1 50090-6074 HUMAN PRESCRIPTION DRUG Divalproex sodium Divalproex sodium TABLET, FILM COATED, EXTENDED RELEASE ORAL 20220914 N/A ANDA ANDA202419 A-S Medication Solutions DIVALPROEX SODIUM 500 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6074-1)
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