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
71610-205-30	71610-205	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181213	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-30)
71610-205-53	71610-205	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181213	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-53)
71610-205-60	71610-205	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181213	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-60)
71610-205-70	71610-205	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181213	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-70)
71610-205-80	71610-205	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181213	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-205-80)
65862-594-01	65862-594	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140602	N/A	ANDA	ANDA202419	Aurobindo Pharma Limited	DIVALPROEX SODIUM	250 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-01)
65862-594-05	65862-594	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140602	N/A	ANDA	ANDA202419	Aurobindo Pharma Limited	DIVALPROEX SODIUM	250 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-594-05)
65862-594-10	65862-594	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140602	N/A	ANDA	ANDA202419	Aurobindo Pharma Limited	DIVALPROEX SODIUM	250 mg/1	10 BLISTER PACK in 1 CARTON (65862-594-10) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
72162-2516-1	72162-2516	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250609	N/A	ANDA	ANDA202419	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2516-1)
72162-2516-5	72162-2516	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250609	N/A	ANDA	ANDA202419	Bryant Ranch Prepack	DIVALPROEX SODIUM	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-2516-5)
71610-289-30	71610-289	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190605	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-30)
71610-289-60	71610-289	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190605	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-60)
71610-289-75	71610-289	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190605	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-75)
71610-289-80	71610-289	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240903	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-80)
71610-289-92	71610-289	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20240903	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-289-92)
50090-4737-0	50090-4737	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20191120	N/A	ANDA	ANDA202419	A-S Medication Solutions	DIVALPROEX SODIUM	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-4737-0)
50090-6074-0	50090-6074	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220914	N/A	ANDA	ANDA202419	A-S Medication Solutions	DIVALPROEX SODIUM	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6074-0)
50090-6074-1	50090-6074	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20220914	N/A	ANDA	ANDA202419	A-S Medication Solutions	DIVALPROEX SODIUM	500 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-6074-1)
71610-157-60	71610-157	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180920	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-157-60)
71610-157-75	71610-157	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180920	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-157-75)