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
71205-530-90	71205-530	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20210203	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	90 TABLET in 1 BOTTLE (71205-530-90)
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)
67296-2137-3	67296-2137	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Redpharm Drug	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (67296-2137-3)
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)
70518-4047-1	70518-4047	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20240516	N/A	ANDA	ANDA078420	REMEDYREPACK INC.	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (70518-4047-1)
70518-4047-0	70518-4047	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20240407	N/A	ANDA	ANDA078420	REMEDYREPACK INC.	NABUMETONE	750 mg/1	14 TABLET in 1 BOTTLE, PLASTIC (70518-4047-0)
76420-210-14	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	14 TABLET in 1 BOTTLE (76420-210-14)
76420-210-30	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (76420-210-30)
76420-210-60	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (76420-210-60)
76420-210-07	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	7 TABLET in 1 BOTTLE (76420-210-07)
76420-210-20	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	20 TABLET in 1 BOTTLE (76420-210-20)
76420-210-10	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	10 TABLET in 1 BOTTLE (76420-210-10)
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)
71205-977-72	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)
71205-978-00	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (71205-978-00)
71205-978-30	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (71205-978-30)
71205-978-55	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (71205-978-55)
71205-978-60	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (71205-978-60)
71205-978-72	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	120 TABLET in 1 BOTTLE, PLASTIC (71205-978-72)