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
80425-0524-2	80425-0524	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20250529	N/A	ANDA	ANDA207466	Advanced Rx of Tennessee, LLC	METAXALONE	800 mg/1	60 TABLET in 1 BOTTLE (80425-0524-2)
68788-8678-1	68788-8678	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20240528	N/A	ANDA	ANDA207466	Preferred Pharmaceuticals Inc.	METAXALONE	800 mg/1	100 TABLET in 1 BOTTLE (68788-8678-1)
68788-8678-9	68788-8678	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20240528	N/A	ANDA	ANDA207466	Preferred Pharmaceuticals Inc.	METAXALONE	800 mg/1	90 TABLET in 1 BOTTLE (68788-8678-9)
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)
51655-171-52	51655-171	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20230203	N/A	ANDA	ANDA207466	Northwind Health Company, LLC	METAXALONE	800 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-171-52)
51655-171-20	51655-171	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20220721	N/A	ANDA	ANDA207466	Northwind Health Company, LLC	METAXALONE	800 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (51655-171-20)