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
70518-2036-0	70518-2036	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20190424	N/A	ANDA	ANDA203730	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	100 POUCH in 1 BOX (70518-2036-0) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-2036-1)
70518-2036-2	70518-2036	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20200104	N/A	ANDA	ANDA203730	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2036-2)
0904-7181-45	0904-7181	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20150601	N/A	ANDA	ANDA203730	Major Pharmaceuticals	DIVALPROEX SODIUM	250 mg/1	80 BLISTER PACK in 1 CARTON (0904-7181-45) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0904-7181-61	0904-7181	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20150601	N/A	ANDA	ANDA203730	Major Pharmaceuticals	DIVALPROEX SODIUM	250 mg/1	100 BLISTER PACK in 1 CARTON (0904-7181-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0904-7182-45	0904-7182	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20150601	N/A	ANDA	ANDA203730	Major Pharmaceuticals	DIVALPROEX SODIUM	500 mg/1	80 BLISTER PACK in 1 CARTON (0904-7182-45) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
0904-7182-61	0904-7182	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20150601	N/A	ANDA	ANDA203730	Major Pharmaceuticals	DIVALPROEX SODIUM	500 mg/1	100 BLISTER PACK in 1 CARTON (0904-7182-61) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
70518-2510-2	70518-2510	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20200309	N/A	ANDA	ANDA203730	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-2510-2)
70518-2510-4	70518-2510	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20200930	N/A	ANDA	ANDA203730	REMEDYREPACK INC.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-2510-4)
65162-755-10	65162-755	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20150601	N/A	ANDA	ANDA203730	Amneal Pharmaceuticals LLC	DIVALPROEX SODIUM	250 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-755-10)
65162-755-50	65162-755	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20150601	N/A	ANDA	ANDA203730	Amneal Pharmaceuticals LLC	DIVALPROEX SODIUM	250 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-755-50)
65162-757-10	65162-757	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20150601	N/A	ANDA	ANDA203730	Amneal Pharmaceuticals LLC	DIVALPROEX SODIUM	500 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-757-10)
65162-757-50	65162-757	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20150601	N/A	ANDA	ANDA203730	Amneal Pharmaceuticals LLC	DIVALPROEX SODIUM	500 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-757-50)
55154-2345-0	55154-2345	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20150601	N/A	ANDA	ANDA203730	Cardinal Health 107, LLC	DIVALPROEX SODIUM	500 mg/1	10 BLISTER PACK in 1 BAG (55154-2345-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
50268-259-15	50268-259	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20220916	N/A	ANDA	ANDA203730	AvPAK	DIVALPROEX SODIUM	250 mg/1	50 BLISTER PACK in 1 BOX (50268-259-15) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-259-11)
50268-260-13	50268-260	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20220916	N/A	ANDA	ANDA203730	AvPAK	DIVALPROEX SODIUM	500 mg/1	30 BLISTER PACK in 1 BOX (50268-260-13) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (50268-260-11)
70518-1556-0	70518-1556	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20181019	N/A	ANDA	ANDA203730	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-1556-0)
70518-1556-1	70518-1556	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20190710	N/A	ANDA	ANDA203730	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	100 POUCH in 1 BOX (70518-1556-1) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-1556-2)
70518-1556-3	70518-1556	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20221107	N/A	ANDA	ANDA203730	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	100 POUCH in 1 BOX (70518-1556-3) / 1 TABLET, EXTENDED RELEASE in 1 POUCH (70518-1556-4)
70518-1556-5	70518-1556	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, EXTENDED RELEASE	ORAL	20240629	N/A	ANDA	ANDA203730	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-1556-5)