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
16571-201-06	16571-201	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20080819	N/A	ANDA	ANDA077863	Rising Pharma Holdings, Inc.	DICLOFENAC SODIUM	75 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (16571-201-06)
16571-201-10	16571-201	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20080819	N/A	ANDA	ANDA077863	Rising Pharma Holdings, Inc.	DICLOFENAC SODIUM	75 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-10)
16571-201-11	16571-201	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20080819	N/A	ANDA	ANDA077863	Rising Pharma Holdings, Inc.	DICLOFENAC SODIUM	75 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-11)
16571-201-50	16571-201	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20080819	N/A	ANDA	ANDA077863	Rising Pharma Holdings, Inc.	DICLOFENAC SODIUM	75 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-50)
76420-670-00	76420-670	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20260325	N/A	ANDA	ANDA077863	Asclemed USA, Inc.	DICLOFENAC SODIUM	75 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-00)
76420-670-01	76420-670	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20240307	N/A	ANDA	ANDA077863	Asclemed USA, Inc.	DICLOFENAC SODIUM	75 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-01)
76420-670-05	76420-670	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20260325	N/A	ANDA	ANDA077863	Asclemed USA, Inc.	DICLOFENAC SODIUM	75 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-05)
76420-670-30	76420-670	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20240307	N/A	ANDA	ANDA077863	Asclemed USA, Inc.	DICLOFENAC SODIUM	75 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-30)
85509-1201-3	85509-1201	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20260107	N/A	ANDA	ANDA077863	PHOENIX RX LLC	DICLOFENAC SODIUM	75 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1201-3)
85509-1201-6	85509-1201	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20260107	N/A	ANDA	ANDA077863	PHOENIX RX LLC	DICLOFENAC SODIUM	75 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (85509-1201-6)
85509-1201-9	85509-1201	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20260107	N/A	ANDA	ANDA077863	PHOENIX RX LLC	DICLOFENAC SODIUM	75 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1201-9)
71335-0456-0	71335-0456	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20090824	N/A	ANDA	ANDA077863	Bryant Ranch Prepack	DICLOFENAC SODIUM	75 mg/1	40 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-0)
71335-0456-1	71335-0456	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20090824	N/A	ANDA	ANDA077863	Bryant Ranch Prepack	DICLOFENAC SODIUM	75 mg/1	28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-1)
71335-0456-2	71335-0456	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20090824	N/A	ANDA	ANDA077863	Bryant Ranch Prepack	DICLOFENAC SODIUM	75 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-2)
71335-0456-3	71335-0456	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20090824	N/A	ANDA	ANDA077863	Bryant Ranch Prepack	DICLOFENAC SODIUM	75 mg/1	20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-3)
71335-0456-4	71335-0456	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20090824	N/A	ANDA	ANDA077863	Bryant Ranch Prepack	DICLOFENAC SODIUM	75 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-4)
68001-281-00	68001-281	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20151221	N/A	ANDA	ANDA077863	BluePoint Laboratories	DICLOFENAC SODIUM	75 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-00)
68001-281-03	68001-281	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20151221	N/A	ANDA	ANDA077863	BluePoint Laboratories	DICLOFENAC SODIUM	75 mg/1	500 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-03)
68001-281-06	68001-281	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20151221	N/A	ANDA	ANDA077863	BluePoint Laboratories	DICLOFENAC SODIUM	75 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-281-06)
68001-281-08	68001-281	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20151221	N/A	ANDA	ANDA077863	BluePoint Laboratories	DICLOFENAC SODIUM	75 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-08)