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
63187-714-15	63187-714	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20160601	N/A	ANDA	ANDA090066	Proficient Rx LP	DICLOFENAC SODIUM	50 mg/1	15 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-714-15)
63187-714-30	63187-714	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20160601	N/A	ANDA	ANDA090066	Proficient Rx LP	DICLOFENAC SODIUM	50 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-714-30)
63187-714-60	63187-714	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20160601	N/A	ANDA	ANDA090066	Proficient Rx LP	DICLOFENAC SODIUM	50 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-714-60)
63187-714-90	63187-714	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20160601	N/A	ANDA	ANDA090066	Proficient Rx LP	DICLOFENAC SODIUM	50 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-714-90)
76420-572-01	76420-572	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20240307	N/A	ANDA	ANDA090066	Asclemed USA, Inc.	DICLOFENAC SODIUM	50 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-01)
76420-572-30	76420-572	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20240307	N/A	ANDA	ANDA090066	Asclemed USA, Inc.	DICLOFENAC SODIUM	50 mg/1	30 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-30)
76420-572-60	76420-572	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20240307	N/A	ANDA	ANDA090066	Asclemed USA, Inc.	DICLOFENAC SODIUM	50 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-60)
76420-572-90	76420-572	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20240307	N/A	ANDA	ANDA090066	Asclemed USA, Inc.	DICLOFENAC SODIUM	50 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-572-90)
76420-571-01	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	100 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-571-01)
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)
68001-279-00	68001-279	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20151221	N/A	ANDA	ANDA090066	BluePoint Laboratories	DICLOFENAC SODIUM	25 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-279-00)
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)
80425-0102-2	80425-0102	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20101231	N/A	ANDA	ANDA090066	Advanced Rx Pharmacy of Tennessee, LLC	DICLOFENAC SODIUM	50 mg/1	60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0102-2)
80425-0102-3	80425-0102	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20101231	N/A	ANDA	ANDA090066	Advanced Rx Pharmacy of Tennessee, LLC	DICLOFENAC SODIUM	50 mg/1	90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0102-3)
68001-280-00	68001-280	HUMAN PRESCRIPTION DRUG	Diclofenac Sodium	Diclofenac Sodium	TABLET, DELAYED RELEASE	ORAL	20151221	N/A	ANDA	ANDA090066	BluePoint Laboratories	DICLOFENAC SODIUM	50 mg/1	100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-00)