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
71205-977-30	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)
71335-1391-1	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191209	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	20 TABLET in 1 BOTTLE (71335-1391-1)
71335-1391-2	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191220	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (71335-1391-2)
71335-1391-3	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191114	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (71335-1391-3)
71335-1391-4	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191107	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (71335-1391-4)
51655-733-52	51655-733	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20210707	N/A	ANDA	ANDA078420	Northwind Health Company, LLC	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-733-52)
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)
55700-845-60	55700-845	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200228	20270331	ANDA	ANDA078420	Quality Care Products, LLC	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (55700-845-60)
80425-0054-1	80425-0054	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Advanced Rx of Tennessee, LLC	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (80425-0054-1)
80425-0054-2	80425-0054	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Advanced Rx of Tennessee, LLC	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (80425-0054-2)
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)
60760-369-14	60760-369	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191010	N/A	ANDA	ANDA078420	St. Mary's Medical Park Pharmacy	NABUMETONE	750 mg/1	14 TABLET in 1 BOTTLE, PLASTIC (60760-369-14)
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)
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)