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
27241-115-01	27241-115	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20200515	N/A	ANDA	ANDA213181	Ajanta Pharma USA Inc.	DIVALPROEX SODIUM	125 mg/1	100 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-01)
27241-115-05	27241-115	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20200515	N/A	ANDA	ANDA213181	Ajanta Pharma USA Inc.	DIVALPROEX SODIUM	125 mg/1	500 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-05)
27241-115-10	27241-115	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20200515	N/A	ANDA	ANDA213181	Ajanta Pharma USA Inc.	DIVALPROEX SODIUM	125 mg/1	1000 CAPSULE, COATED PELLETS in 1 BOTTLE (27241-115-10)
70518-3457-0	70518-3457	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20220720	N/A	ANDA	ANDA213181	REMEDYREPACK INC.	DIVALPROEX SODIUM	125 mg/1	100 POUCH in 1 BOX (70518-3457-0) / 1 CAPSULE, COATED PELLETS in 1 POUCH (70518-3457-1)
70518-3457-2	70518-3457	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20230801	N/A	ANDA	ANDA213181	REMEDYREPACK INC.	DIVALPROEX SODIUM	125 mg/1	100 POUCH in 1 BOX (70518-3457-2) / 1 CAPSULE, COATED PELLETS in 1 POUCH (70518-3457-3)