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
70756-447-11	70756-447	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20250812	N/A	ANDA	ANDA217358	Lifestar Pharma LLC	DIVALPROEX SODIUM	125 mg/1	100 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-11)
70756-447-12	70756-447	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20250812	N/A	ANDA	ANDA217358	Lifestar Pharma LLC	DIVALPROEX SODIUM	125 mg/1	1000 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-12)
70756-447-30	70756-447	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20250812	N/A	ANDA	ANDA217358	Lifestar Pharma LLC	DIVALPROEX SODIUM	125 mg/1	30 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-30)
70756-447-51	70756-447	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20250812	N/A	ANDA	ANDA217358	Lifestar Pharma LLC	DIVALPROEX SODIUM	125 mg/1	500 CAPSULE, COATED PELLETS in 1 BOTTLE (70756-447-51)
81469-492-01	81469-492	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20251110	N/A	ANDA	ANDA217358	First Nation Group, LLC	DIVALPROEX SODIUM	125 mg/1	100 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-01)
81469-492-10	81469-492	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	CAPSULE, COATED PELLETS	ORAL	20251110	N/A	ANDA	ANDA217358	First Nation Group, LLC	DIVALPROEX SODIUM	125 mg/1	1000 CAPSULE, COATED PELLETS in 1 BOTTLE (81469-492-10)