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
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)
72162-1558-1	72162-1558	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20240208	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE (72162-1558-1)
72162-1558-5	72162-1558	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20240208	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE (72162-1558-5)
50090-5294-0	50090-5294	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20201023	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (50090-5294-0)
50090-5294-7	50090-5294	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20201023	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (50090-5294-7)
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)
63629-8509-1	63629-8509	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE (63629-8509-1)
72189-072-14	72189-072	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20200618	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	750 mg/1	14 TABLET in 1 BOTTLE (72189-072-14)
72189-072-30	72189-072	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20200618	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (72189-072-30)
72189-072-60	72189-072	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20200618	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (72189-072-60)
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)
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)
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)