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）

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
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)
70518-1781-0	70518-1781	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190107	N/A	ANDA	ANDA202419	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-1781-0)
70518-1781-1	70518-1781	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200803	N/A	ANDA	ANDA202419	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	100 POUCH in 1 BOX (70518-1781-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-1781-2)
70518-1897-0	70518-1897	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190222	N/A	ANDA	ANDA202419	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-1897-0)
70518-1897-1	70518-1897	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190222	N/A	ANDA	ANDA202419	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	100 POUCH in 1 BOX (70518-1897-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-1897-2)
70518-2003-0	70518-2003	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190408	N/A	ANDA	ANDA202419	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2003-0)
70518-2003-1	70518-2003	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191209	N/A	ANDA	ANDA202419	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	100 POUCH in 1 BOX (70518-2003-1) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 POUCH (70518-2003-2)
50090-6074-0	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	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6074-0)
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)
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)
65862-594-05	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)
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
71610-157-60	71610-157	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180920	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-157-60)
71610-157-75	71610-157	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180920	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-157-75)