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
71205-977-00	71205-977	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	500 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (71205-977-00)
71205-977-30	71205-977	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (71205-977-30)
71205-977-55	71205-977	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (71205-977-55)
71205-977-60	71205-977	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (71205-977-60)
71205-977-72	71205-977	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	500 mg/1	120 TABLET in 1 BOTTLE, PLASTIC (71205-977-72)
71205-977-90	71205-977	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (71205-977-90)
72789-040-30	72789-040	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191217	N/A	ANDA	ANDA078420	PD-Rx Pharmaceuticals, Inc.	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-040-30)
71335-1559-0	71335-1559	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220210	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	7 TABLET in 1 BOTTLE (71335-1559-0)
71335-1559-1	71335-1559	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220210	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (71335-1559-1)
70518-3835-0	70518-3835	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20230818	N/A	ANDA	ANDA078420	REMEDYREPACK INC.	NABUMETONE	500 mg/1	14 TABLET in 1 BOTTLE, PLASTIC (70518-3835-0)
70518-3835-1	70518-3835	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20240312	N/A	ANDA	ANDA078420	REMEDYREPACK INC.	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (70518-3835-1)
71335-2293-1	71335-2293	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20231201	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE (71335-2293-1)
68788-7597-3	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (68788-7597-3)
68788-7597-6	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (68788-7597-6)
68788-7597-8	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	120 TABLET in 1 BOTTLE (68788-7597-8)
68788-7597-9	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	90 TABLET in 1 BOTTLE (68788-7597-9)
68788-7597-1	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE (68788-7597-1)
68788-7597-2	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	20 TABLET in 1 BOTTLE (68788-7597-2)
71335-2292-1	71335-2292	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20231201	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE (71335-2292-1)
80425-0104-1	80425-0104	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Advanced Rx Pharmacy of Tennessee, LLC	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (80425-0104-1)