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
60687-879-61	60687-879	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20250206	N/A	ANDA	ANDA079163	American Health Packaging	DIVALPROEX SODIUM	500 mg/1	90 BLISTER PACK in 1 CARTON (60687-879-61) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-879-11)
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)
29300-140-10	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)
71335-2124-1	71335-2124	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220719	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-1)
71335-2124-2	71335-2124	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220719	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-2)
71335-2124-3	71335-2124	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220719	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-3)
71335-2124-4	71335-2124	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20220719	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71335-2124-4)
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)
63187-742-30	63187-742	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20161003	N/A	ANDA	ANDA079163	Proficient Rx LP	DIVALPROEX SODIUM	250 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-30)
63187-742-60	63187-742	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20161003	N/A	ANDA	ANDA079163	Proficient Rx LP	DIVALPROEX SODIUM	250 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-60)
63187-742-90	63187-742	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20161003	N/A	ANDA	ANDA079163	Proficient Rx LP	DIVALPROEX SODIUM	250 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (63187-742-90)
63629-4278-1	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20211222	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-1)
63629-4278-2	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20121119	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-2)
63629-4278-3	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20141110	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-3)
63629-4278-4	63629-4278	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20180531	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	180 TABLET, DELAYED RELEASE in 1 BOTTLE (63629-4278-4)
71335-2885-1	71335-2885	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	Divalproex Sodium	TABLET, DELAYED RELEASE	ORAL	20251023	N/A	ANDA	ANDA079163	Bryant Ranch Prepack	DIVALPROEX SODIUM	250 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2885-1)
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)
29300-139-05	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)