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
69452-433-13	69452-433	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	125 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-13)
69452-433-20	69452-433	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	125 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-20)
69452-433-30	69452-433	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-433-30)
69452-434-13	69452-434	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-434-13)
69452-434-20	69452-434	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-434-20)
69452-434-30	69452-434	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-434-30)
69452-435-13	69452-435	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-13)
69452-435-20	69452-435	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-20)
69452-435-30	69452-435	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20240626	N/A	ANDA	ANDA078853	Bionpharma Inc.	DIVALPROEX SODIUM	500 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (69452-435-30)