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
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)
60760-368-15	60760-368	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191021	N/A	ANDA	ANDA078420	St. Mary's Medical Park Pharmacy	NABUMETONE	500 mg/1	15 TABLET in 1 BOTTLE, PLASTIC (60760-368-15)
60760-368-60	60760-368	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200303	N/A	ANDA	ANDA078420	St. Mary's Medical Park Pharmacy	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (60760-368-60)
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)
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)
69367-241-01	69367-241	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190925	N/A	ANDA	ANDA078420	Westminster Pharmaceuticals, LLC	NABUMETONE	500 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (69367-241-01)
69367-241-05	69367-241	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190925	N/A	ANDA	ANDA078420	Westminster Pharmaceuticals, LLC	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (69367-241-05)
69367-242-01	69367-242	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190925	N/A	ANDA	ANDA078420	Westminster Pharmaceuticals, LLC	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (69367-242-01)
69367-242-05	69367-242	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190925	N/A	ANDA	ANDA078420	Westminster Pharmaceuticals, LLC	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (69367-242-05)
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)
72189-184-14	72189-184	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20210511	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	500 mg/1	14 TABLET in 1 BOTTLE (72189-184-14)
72189-184-30	72189-184	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20210511	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (72189-184-30)
72189-184-60	72189-184	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20210511	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (72189-184-60)
72189-184-90	72189-184	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20210511	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (72189-184-90)
72789-540-14	72789-540	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20251223	N/A	ANDA	ANDA078420	PD-Rx Pharmaceuticals, Inc.	NABUMETONE	750 mg/1	14 TABLET in 1 BOTTLE, PLASTIC (72789-540-14)
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)