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
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)
60687-868-01	60687-868	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250321	N/A	ANDA	ANDA079163	American Health Packaging	DIVALPROEX SODIUM	250 mg/1	100 BLISTER PACK in 1 CARTON (60687-868-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-868-11)
29300-138-05	29300-138	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-05)
29300-138-10	29300-138	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	125 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-10)
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)
68001-474-00	68001-474	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20210120	N/A	ANDA	ANDA079163	BluePoint Laboratories	DIVALPROEX SODIUM	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-474-00)
68001-474-03	68001-474	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20210120	N/A	ANDA	ANDA079163	BluePoint Laboratories	DIVALPROEX SODIUM	500 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-474-03)
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)
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)
29300-139-05	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	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-05)
29300-139-10	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	1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-10)