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
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)
71335-2885-1	71335-2885	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20251023	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2885-1)
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)
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)
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)