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
60687-904-01	60687-904	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20251201	N/A	ANDA	ANDA214643	American Health Packaging	DIVALPROEX SODIUM	250 mg/1	100 BLISTER PACK in 1 CARTON (60687-904-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-904-11)
68001-647-00	68001-647	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250806	N/A	ANDA	ANDA214643	BluePoint Laboratories	DIVALPROEX SODIUM	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-647-00)
68001-647-03	68001-647	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250806	N/A	ANDA	ANDA214643	BluePoint Laboratories	DIVALPROEX SODIUM	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-647-03)
67046-1595-3	67046-1595	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250916	N/A	ANDA	ANDA214643	Coupler LLC	DIVALPROEX SODIUM	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (67046-1595-3)
29300-380-01	29300-380	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220715	N/A	ANDA	ANDA214643	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-380-01)
29300-380-05	29300-380	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220715	N/A	ANDA	ANDA214643	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	250 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-380-05)
29300-381-01	29300-381	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220715	N/A	ANDA	ANDA214643	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-01)
29300-381-05	29300-381	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220715	N/A	ANDA	ANDA214643	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (29300-381-05)
68001-646-00	68001-646	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250807	N/A	ANDA	ANDA214643	BluePoint Laboratories	DIVALPROEX SODIUM	250 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-646-00)
68001-646-03	68001-646	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250710	N/A	ANDA	ANDA214643	BluePoint Laboratories	DIVALPROEX SODIUM	250 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-646-03)
60687-915-01	60687-915	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20251201	N/A	ANDA	ANDA214643	American Health Packaging	DIVALPROEX SODIUM	500 mg/1	100 BLISTER PACK in 1 CARTON (60687-915-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-915-11)
60687-915-02	60687-915	HUMAN PRESCRIPTION DRUG	divalproex sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20251201	N/A	ANDA	ANDA214643	American Health Packaging	DIVALPROEX SODIUM	500 mg/1	80 BLISTER PACK in 1 CARTON (60687-915-02) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-915-93)