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
46708-821-10	46708-821	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, DELAYED RELEASE	ORAL	20241223	N/A	ANDA	ANDA218793	Alembic Pharmaceuticals Limited	DIVALPROEX SODIUM	125 mg/1	100 BLISTER PACK in 1 CARTON (46708-821-10) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
46708-821-31	46708-821	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, DELAYED RELEASE	ORAL	20241223	N/A	ANDA	ANDA218793	Alembic Pharmaceuticals Limited	DIVALPROEX SODIUM	125 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-821-31)
46708-821-91	46708-821	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, DELAYED RELEASE	ORAL	20241223	N/A	ANDA	ANDA218793	Alembic Pharmaceuticals Limited	DIVALPROEX SODIUM	125 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-821-91)
62332-821-10	62332-821	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, DELAYED RELEASE	ORAL	20241223	N/A	ANDA	ANDA218793	Alembic Pharmaceuticals Inc.	DIVALPROEX SODIUM	125 mg/1	100 BLISTER PACK in 1 CARTON (62332-821-10) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK
62332-821-31	62332-821	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, DELAYED RELEASE	ORAL	20241223	N/A	ANDA	ANDA218793	Alembic Pharmaceuticals Inc.	DIVALPROEX SODIUM	125 mg/1	100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-31)
62332-821-71	62332-821	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, DELAYED RELEASE	ORAL	20250321	N/A	ANDA	ANDA218793	Alembic Pharmaceuticals Inc.	DIVALPROEX SODIUM	125 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-71)
62332-821-91	62332-821	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	CAPSULE, DELAYED RELEASE	ORAL	20241223	N/A	ANDA	ANDA218793	Alembic Pharmaceuticals Inc.	DIVALPROEX SODIUM	125 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-821-91)