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
71205-978-72	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)
60760-369-60	60760-369	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200127	N/A	ANDA	ANDA078420	St. Mary's Medical Park Pharmacy	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (60760-369-60)
55700-840-60	55700-840	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200124	20270531	ANDA	ANDA078420	Quality Care Products, LLC	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (55700-840-60)
50228-466-01	50228-466	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE (50228-466-01)
50228-466-05	50228-466	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE (50228-466-05)
50228-466-30	50228-466	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (50228-466-30)
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)
60760-369-90	60760-369	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20210223	N/A	ANDA	ANDA078420	St. Mary's Medical Park Pharmacy	NABUMETONE	750 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (60760-369-90)
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)
63629-8506-1	63629-8506	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE (63629-8506-1)
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)
50090-5294-8	50090-5294	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20201023	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (50090-5294-8)
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)
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)
70518-4047-2	70518-4047	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20260223	N/A	ANDA	ANDA078420	REMEDYREPACK INC.	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (70518-4047-2)
50090-6167-0	50090-6167	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20221013	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (50090-6167-0)
50090-6167-2	50090-6167	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20221013	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	750 mg/1	14 TABLET in 1 BOTTLE (50090-6167-2)
50090-6167-3	50090-6167	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20221013	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (50090-6167-3)
50090-6167-4	50090-6167	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20221013	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	750 mg/1	20 TABLET in 1 BOTTLE (50090-6167-4)