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
71610-289-60	71610-289	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190605	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-60)
71610-289-75	71610-289	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190605	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-75)
71610-289-80	71610-289	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240903	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-80)
71610-289-92	71610-289	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240903	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-92)