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
31722-022-05	31722-022	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230926	N/A	ANDA	ANDA215527	Camber Pharmaceuticals, Inc.	DIVALPROEX SODIUM	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-022-05)
31722-022-01	31722-022	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230926	N/A	ANDA	ANDA215527	Camber Pharmaceuticals, Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-022-01)
31722-021-05	31722-021	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230926	N/A	ANDA	ANDA215527	Camber Pharmaceuticals, Inc.	DIVALPROEX SODIUM	250 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-021-05)
31722-021-01	31722-021	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230926	N/A	ANDA	ANDA215527	Camber Pharmaceuticals, Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-021-01)