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
72789-028-30	72789-028	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20191111	N/A	ANDA	ANDA207466	PD-Rx Pharmaceuticals, Inc.	METAXALONE	800 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-028-30)
72789-028-15	72789-028	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20191119	N/A	ANDA	ANDA207466	PD-Rx Pharmaceuticals, Inc.	METAXALONE	800 mg/1	15 TABLET in 1 BOTTLE, PLASTIC (72789-028-15)
0276-0508-10	0276-0508	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20211101	N/A	ANDA	ANDA207466	Misemer Pharmaceuticals, Inc.	METAXALONE	400 mg/1	100 TABLET in 1 BOTTLE (0276-0508-10)
55111-650-01	55111-650	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20170831	N/A	ANDA	ANDA207466	Dr. Reddy’s Laboratories Limited	METAXALONE	800 mg/1	100 TABLET in 1 BOTTLE (55111-650-01)
0904-6831-04	0904-6831	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20170831	N/A	ANDA	ANDA207466	Major Pharmaceuticals	METAXALONE	800 mg/1	30 BLISTER PACK in 1 CARTON (0904-6831-04) / 1 TABLET in 1 BLISTER PACK
0904-6831-06	0904-6831	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20170831	N/A	ANDA	ANDA207466	Major Pharmaceuticals	METAXALONE	800 mg/1	50 BLISTER PACK in 1 CARTON (0904-6831-06) / 1 TABLET in 1 BLISTER PACK
68001-485-00	68001-485	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20210531	N/A	ANDA	ANDA207466	BluePoint Laboratories	METAXALONE	800 mg/1	100 TABLET in 1 BOTTLE (68001-485-00)
60687-663-21	60687-663	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20230106	N/A	ANDA	ANDA207466	American Health Packaging	METAXALONE	800 mg/1	30 BLISTER PACK in 1 CARTON (60687-663-21) / 1 TABLET in 1 BLISTER PACK (60687-663-11)
71205-016-10	71205-016	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20180402	N/A	ANDA	ANDA207466	Proficient Rx LP	METAXALONE	800 mg/1	10 TABLET in 1 BOTTLE (71205-016-10)
71205-016-30	71205-016	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20180402	N/A	ANDA	ANDA207466	Proficient Rx LP	METAXALONE	800 mg/1	30 TABLET in 1 BOTTLE (71205-016-30)
71205-016-60	71205-016	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20180402	N/A	ANDA	ANDA207466	Proficient Rx LP	METAXALONE	800 mg/1	60 TABLET in 1 BOTTLE (71205-016-60)
71205-016-90	71205-016	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20180402	N/A	ANDA	ANDA207466	Proficient Rx LP	METAXALONE	800 mg/1	90 TABLET in 1 BOTTLE (71205-016-90)
50228-323-01	50228-323	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20170831	N/A	ANDA	ANDA207466	ScieGen Pharmaceuticals, Inc.	METAXALONE	800 mg/1	100 TABLET in 1 BOTTLE (50228-323-01)
50228-323-05	50228-323	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20170831	N/A	ANDA	ANDA207466	ScieGen Pharmaceuticals, Inc.	METAXALONE	800 mg/1	500 TABLET in 1 BOTTLE (50228-323-05)
50228-323-30	50228-323	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20170831	N/A	ANDA	ANDA207466	ScieGen Pharmaceuticals, Inc.	METAXALONE	800 mg/1	30 TABLET in 1 BOTTLE (50228-323-30)
50228-474-30	50228-474	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200430	N/A	ANDA	ANDA207466	ScieGen Pharmaceuticals, Inc.	METAXALONE	400 mg/1	30 TABLET in 1 BOTTLE (50228-474-30)
69097-998-07	69097-998	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20230612	N/A	ANDA	ANDA207466	CIPLA USA INC.	METAXALONE	400 mg/1	100 TABLET in 1 BOTTLE (69097-998-07)
51655-171-20	51655-171	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20220721	N/A	ANDA	ANDA207466	Northwind Pharmaceuticals, LLC	METAXALONE	800 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (51655-171-20)
51655-171-52	51655-171	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20230203	N/A	ANDA	ANDA207466	Northwind Pharmaceuticals, LLC	METAXALONE	800 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-171-52)
50228-474-10	50228-474	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200430	N/A	ANDA	ANDA207466	ScieGen Pharmaceuticals, Inc.	METAXALONE	400 mg/1	1000 TABLET in 1 BOTTLE (50228-474-10)