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
61919-249-60	61919-249	HUMAN PRESCRIPTION DRUG	DIVALPROEX SODIUM	divalproex sodium	TABLET, DELAYED RELEASE	ORAL	20220406	N/A	ANDA	ANDA079163	DirectRx	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (61919-249-60)
71335-0008-4	71335-0008	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20211227	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-4)
71335-0008-3	71335-0008	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20180301	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-3)
71335-0008-2	71335-0008	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20180306	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-2)
71335-0008-1	71335-0008	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20181221	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0008-1)
29300-138-01	29300-138	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	125 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-01)
29300-139-05	29300-139	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-05)
29300-139-10	29300-139	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	250 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-10)
29300-140-01	29300-140	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-01)
29300-140-05	29300-140	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	500 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-05)
29300-138-05	29300-138	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	125 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-05)
29300-138-10	29300-138	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	125 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-138-10)
29300-139-01	29300-139	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-139-01)
29300-140-10	29300-140	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20111001	N/A	ANDA	ANDA079163	Unichem Pharmaceuticals (USA), Inc.	DIVALPROEX SODIUM	500 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (29300-140-10)
70518-3620-4	70518-3620	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20230313	N/A	ANDA	ANDA079163	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3620-4)
50090-2007-0	50090-2007	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20150918	N/A	ANDA	ANDA079163	A-S Medication Solutions	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-2007-0)
50090-2007-1	50090-2007	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20170802	N/A	ANDA	ANDA079163	A-S Medication Solutions	DIVALPROEX SODIUM	250 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-2007-1)
70518-3620-0	70518-3620	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20230121	N/A	ANDA	ANDA079163	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	100 POUCH in 1 BOX (70518-3620-0) / 1 TABLET, DELAYED RELEASE in 1 POUCH (70518-3620-1)
70518-3620-2	70518-3620	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20230131	N/A	ANDA	ANDA079163	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3620-2)
70518-3620-3	70518-3620	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20230203	N/A	ANDA	ANDA079163	REMEDYREPACK INC.	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BLISTER PACK (70518-3620-3)