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)
71610-249-30	71610-249	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20200915	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-30)
71610-249-53	71610-249	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190314	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-53)
71610-249-60	71610-249	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190314	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-60)
71610-249-70	71610-249	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190314	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-70)
71610-249-80	71610-249	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20201009	N/A	ANDA	ANDA202419	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71610-249-80)
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)
16714-484-01	16714-484	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140602	N/A	ANDA	ANDA202419	NorthStar Rx LLC	DIVALPROEX SODIUM	250 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-484-01)
16714-484-02	16714-484	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140602	N/A	ANDA	ANDA202419	NorthStar Rx LLC	DIVALPROEX SODIUM	250 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-484-02)
16714-485-01	16714-485	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140602	N/A	ANDA	ANDA202419	NorthStar Rx LLC	DIVALPROEX SODIUM	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-485-01)
16714-485-02	16714-485	HUMAN PRESCRIPTION DRUG	Divalproex sodium	Divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140602	N/A	ANDA	ANDA202419	NorthStar Rx LLC	DIVALPROEX SODIUM	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-485-02)