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
76420-571-30	76420-571	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20240307	N/A	ANDA	ANDA090066	Asclemed USA, Inc.	DICLOFENAC SODIUM	25 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-571-30)
76420-571-60	76420-571	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20240307	N/A	ANDA	ANDA090066	Asclemed USA, Inc.	DICLOFENAC SODIUM	25 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-571-60)
76420-571-90	76420-571	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20240307	N/A	ANDA	ANDA090066	Asclemed USA, Inc.	DICLOFENAC SODIUM	25 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-571-90)
68788-8784-1	68788-8784	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20241212	N/A	ANDA	ANDA090066	Preferred Pharmaceuticals Inc.	DICLOFENAC SODIUM	50 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-1)
68788-8784-3	68788-8784	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20241212	N/A	ANDA	ANDA090066	Preferred Pharmaceuticals Inc.	DICLOFENAC SODIUM	50 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-3)
68788-8784-6	68788-8784	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20241212	N/A	ANDA	ANDA090066	Preferred Pharmaceuticals Inc.	DICLOFENAC SODIUM	50 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-6)
68788-8784-8	68788-8784	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20241212	N/A	ANDA	ANDA090066	Preferred Pharmaceuticals Inc.	DICLOFENAC SODIUM	50 mg/1	120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-8)
68788-8784-9	68788-8784	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20241212	N/A	ANDA	ANDA090066	Preferred Pharmaceuticals Inc.	DICLOFENAC SODIUM	50 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-9)
16571-202-06	16571-202	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20101231	N/A	ANDA	ANDA090066	Rising Pharma Holdings, Inc.	DICLOFENAC SODIUM	50 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-202-06)
16571-202-10	16571-202	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20101231	N/A	ANDA	ANDA090066	Rising Pharma Holdings, Inc.	DICLOFENAC SODIUM	50 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-202-10)
16571-202-11	16571-202	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20101231	N/A	ANDA	ANDA090066	Rising Pharma Holdings, Inc.	DICLOFENAC SODIUM	50 mg/1	1000 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-202-11)
60687-606-01	60687-606	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20220607	N/A	ANDA	ANDA090066	American Health Packaging	DICLOFENAC SODIUM	50 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-606-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-606-11)