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=ANDA078853"
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
71335-2783-1 71335-2783 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20251013 N/A ANDA ANDA078853 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2783-1)
71335-2783-2 71335-2783 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20251013 N/A ANDA ANDA078853 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2783-2)
71335-2783-3 71335-2783 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20251013 N/A ANDA ANDA078853 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2783-3)
71335-2783-4 71335-2783 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20251013 N/A ANDA ANDA078853 Bryant Ranch Prepack DIVALPROEX SODIUM 250 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2783-4)
69452-433-13 69452-433 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20240626 N/A ANDA ANDA078853 Bionpharma Inc. DIVALPROEX SODIUM 125 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-13)
69452-433-20 69452-433 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20240626 N/A ANDA ANDA078853 Bionpharma Inc. DIVALPROEX SODIUM 125 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-20)
69452-433-30 69452-433 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20240626 N/A ANDA ANDA078853 Bionpharma Inc. DIVALPROEX SODIUM 125 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-30)
0615-8586-39 0615-8586 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20250820 N/A ANDA ANDA078853 NCS HealthCare of KY, LLC dba Vangard Labs DIVALPROEX SODIUM 125 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8586-39)
69452-434-13 69452-434 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20240626 N/A ANDA ANDA078853 Bionpharma Inc. DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-434-13)
69452-434-20 69452-434 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20240626 N/A ANDA ANDA078853 Bionpharma Inc. DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-434-20)
69452-434-30 69452-434 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20240626 N/A ANDA ANDA078853 Bionpharma Inc. DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-434-30)
0615-8587-39 0615-8587 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20250815 N/A ANDA ANDA078853 NCS HealthCare of KY, LLC dba Vangard Labs DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8587-39)
82804-233-30 82804-233 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20250806 N/A ANDA ANDA078853 Proficient Rx LP DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (82804-233-30)
69452-435-13 69452-435 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20240626 N/A ANDA ANDA078853 Bionpharma Inc. DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-13)
69452-435-20 69452-435 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20240626 N/A ANDA ANDA078853 Bionpharma Inc. DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-20)
69452-435-30 69452-435 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20240626 N/A ANDA ANDA078853 Bionpharma Inc. DIVALPROEX SODIUM 500 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-30)
0615-8588-39 0615-8588 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20250818 N/A ANDA ANDA078853 NCS HealthCare of KY, LLC dba Vangard Labs DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8588-39)
71335-2782-1 71335-2782 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20250924 N/A ANDA ANDA078853 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-1)
71335-2782-2 71335-2782 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20250924 N/A ANDA ANDA078853 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-2)
71335-2782-3 71335-2782 HUMAN PRESCRIPTION DRUG divalproex sodium divalproex sodium TABLET, DELAYED RELEASE ORAL 20250924 N/A ANDA ANDA078853 Bryant Ranch Prepack DIVALPROEX SODIUM 500 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2782-3)
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