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
71610-030-30	71610-030	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20181112	N/A	ANDA	ANDA077567	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-30)
71610-030-60	71610-030	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180118	N/A	ANDA	ANDA077567	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-60)
71610-030-75	71610-030	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20180209	N/A	ANDA	ANDA077567	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	150 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-75)
71610-030-80	71610-030	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190710	N/A	ANDA	ANDA077567	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-80)
71610-030-92	71610-030	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20190710	N/A	ANDA	ANDA077567	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	250 mg/1	270 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-030-92)
51079-766-08	51079-766	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20090203	N/A	ANDA	ANDA077567	Mylan Institutional Inc.	DIVALPROEX SODIUM	250 mg/1	80 BLISTER PACK in 1 CARTON (51079-766-08) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-766-01)
51079-767-08	51079-767	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20090203	N/A	ANDA	ANDA077567	Mylan Institutional Inc.	DIVALPROEX SODIUM	500 mg/1	80 BLISTER PACK in 1 CARTON (51079-767-08) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-767-01)
71610-707-53	71610-707	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230516	N/A	ANDA	ANDA077567	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-707-53)
71610-707-60	71610-707	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230518	N/A	ANDA	ANDA077567	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-707-60)
71610-707-70	71610-707	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230516	N/A	ANDA	ANDA077567	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-707-70)
71610-707-80	71610-707	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230516	N/A	ANDA	ANDA077567	Aphena Pharma Solutions - Tennessee, LLC	DIVALPROEX SODIUM	500 mg/1	180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-707-80)
0378-0472-01	0378-0472	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20090129	N/A	ANDA	ANDA077567	Mylan Pharmaceuticals Inc.	DIVALPROEX SODIUM	250 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0472-01)
0378-0472-05	0378-0472	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20090129	N/A	ANDA	ANDA077567	Mylan Pharmaceuticals Inc.	DIVALPROEX SODIUM	250 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0472-05)
0378-0473-01	0378-0473	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20090202	N/A	ANDA	ANDA077567	Mylan Pharmaceuticals Inc.	DIVALPROEX SODIUM	500 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0473-01)
0378-0473-05	0378-0473	HUMAN PRESCRIPTION DRUG	Divalproex Sodium	divalproex sodium	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20090202	N/A	ANDA	ANDA077567	Mylan Pharmaceuticals Inc.	DIVALPROEX SODIUM	500 mg/1	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0473-05)