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=ANDA078182"
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
0615-8328-30 0615-8328 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20191203 20240531 ANDA ANDA078182 NCS HealthCare of KY, LLC dba Vangard Labs DIVALPROEX SODIUM 500 mg/1 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8328-30) / 5 TABLET, DELAYED RELEASE in 1 BLISTER PACK
0615-8328-39 0615-8328 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20191205 N/A ANDA ANDA078182 NCS HealthCare of KY, LLC dba Vangard Labs DIVALPROEX SODIUM 500 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8328-39)
70518-3796-0 70518-3796 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230717 N/A ANDA ANDA078182 REMEDYREPACK INC. DIVALPROEX SODIUM 125 mg/1 100 POUCH in 1 BOX (70518-3796-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3796-1)
0832-7122-11 0832-7122 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20140321 N/A ANDA ANDA078182 Upsher-Smith Laboratories, LLC DIVALPROEX SODIUM 125 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7122-11)
0832-7122-15 0832-7122 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20140321 N/A ANDA ANDA078182 Upsher-Smith Laboratories, LLC DIVALPROEX SODIUM 125 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7122-15)
0832-7123-01 0832-7123 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20160401 N/A ANDA ANDA078182 Upsher-Smith Laboratories, LLC DIVALPROEX SODIUM 250 mg/1 100 BLISTER PACK in 1 CARTON (0832-7123-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0832-7123-89)
0832-7123-11 0832-7123 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20140321 N/A ANDA ANDA078182 Upsher-Smith Laboratories, LLC DIVALPROEX SODIUM 250 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7123-11)
0832-7123-15 0832-7123 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20140321 N/A ANDA ANDA078182 Upsher-Smith Laboratories, LLC DIVALPROEX SODIUM 250 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7123-15)
0832-7124-01 0832-7124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20160401 N/A ANDA ANDA078182 Upsher-Smith Laboratories, LLC DIVALPROEX SODIUM 500 mg/1 100 BLISTER PACK in 1 CARTON (0832-7124-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0832-7124-89)
0832-7124-11 0832-7124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20140321 N/A ANDA ANDA078182 Upsher-Smith Laboratories, LLC DIVALPROEX SODIUM 500 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7124-11)
0832-7124-15 0832-7124 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20140321 N/A ANDA ANDA078182 Upsher-Smith Laboratories, LLC DIVALPROEX SODIUM 500 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (0832-7124-15)
71610-031-60 71610-031 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20180119 N/A ANDA ANDA078182 Aphena Pharma Solutions - Tennessee, LLC DIVALPROEX SODIUM 250 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-031-60)
71610-032-53 71610-032 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20180119 N/A ANDA ANDA078182 Aphena Pharma Solutions - Tennessee, LLC DIVALPROEX SODIUM 500 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-53)
71610-032-60 71610-032 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20180119 N/A ANDA ANDA078182 Aphena Pharma Solutions - Tennessee, LLC DIVALPROEX SODIUM 500 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-032-60)
55154-5633-0 55154-5633 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20160401 N/A ANDA ANDA078182 Cardinal Health 107, LLC DIVALPROEX SODIUM 500 mg/1 10 BLISTER PACK in 1 BAG (55154-5633-0) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK
70518-3364-0 70518-3364 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220211 N/A ANDA ANDA078182 REMEDYREPACK INC. DIVALPROEX SODIUM 500 mg/1 100 POUCH in 1 BOX (70518-3364-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3364-1)
70518-3459-0 70518-3459 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20220725 N/A ANDA ANDA078182 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 100 POUCH in 1 BOX (70518-3459-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3459-1)
70518-3459-2 70518-3459 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230709 N/A ANDA ANDA078182 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3459-2)
70518-3459-3 70518-3459 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20230926 N/A ANDA ANDA078182 REMEDYREPACK INC. DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3459-3)
0615-8327-39 0615-8327 HUMAN PRESCRIPTION DRUG Divalproex Sodium Divalproex Sodium TABLET, DELAYED RELEASE ORAL 20200109 N/A ANDA ANDA078182 NCS HealthCare of KY, LLC dba Vangard Labs DIVALPROEX SODIUM 250 mg/1 30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (0615-8327-39)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase