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
71335-2862-1	71335-2862	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20251023	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2862-1)
63629-4278-1	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20211222	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-1)
63629-4278-2	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20121119	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-2)
63629-4278-3	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141110	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-3)
63629-4278-4	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20180531	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-4)
63629-4278-5	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20180917	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-5)
60687-879-61	60687-879	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250206	N/A	ANDA	ANDA079163	American Health Packaging	DIVALPROEX SODIUM	500 mg/1	90 BLISTER PACK in 1 CARTON (60687-879-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-879-11)
29300-139-01	29300-139	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-01)
68001-473-00	68001-473	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20210120	N/A	ANDA	ANDA079163	BluePoint Laboratories	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-473-00)
68001-473-03	68001-473	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20210120	N/A	ANDA	ANDA079163	BluePoint Laboratories	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-473-03)
70518-3620-0	70518-3620	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20230121	N/A	ANDA	ANDA079163	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	100 POUCH in 1 BOX (70518-3620-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3620-1)
60687-857-21	60687-857	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250317	N/A	ANDA	ANDA079163	American Health Packaging	DIVALPROEX SODIUM	125 mg/1	30 BLISTER PACK in 1 CARTON (60687-857-21) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-857-11)
72162-2460-1	72162-2460	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250221	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-1)
72162-2460-3	72162-2460	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250221	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-3)
72162-2460-5	72162-2460	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250221	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-2460-5)
61919-249-30	61919-249	HUMAN PRESCRIPTION DRUG	DIVALPROEX SODIUM	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20220406	N/A	ANDA	ANDA079163	DirectRx	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-30)
61919-249-60	61919-249	HUMAN PRESCRIPTION DRUG	DIVALPROEX SODIUM	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20220406	N/A	ANDA	ANDA079163	DirectRx	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-60)
68001-472-00	68001-472	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20210120	N/A	ANDA	ANDA079163	BluePoint Laboratories	DIVALPROEX SODIUM	125 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-00)
68001-472-03	68001-472	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20210120	N/A	ANDA	ANDA079163	BluePoint Laboratories	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-472-03)
51655-365-52	51655-365	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20200529	N/A	ANDA	ANDA079163	Northwind Health Company, LLC	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-365-52)