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
50090-3670-0	50090-3670	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20181016	N/A	ANDA	ANDA204770	A-S Medication Solutions	METAXALONE	800 mg/1	20 TABLET in 1 BOTTLE (50090-3670-0)
60760-289-06	60760-289	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200616	N/A	ANDA	ANDA204770	St. Mary's Medical Park Pharmacy	METAXALONE	800 mg/1	6 TABLET in 1 BOTTLE, PLASTIC (60760-289-06)
60760-289-20	60760-289	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200331	N/A	ANDA	ANDA204770	St. Mary's Medical Park Pharmacy	METAXALONE	800 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (60760-289-20)
60760-289-30	60760-289	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200331	N/A	ANDA	ANDA204770	St. Mary's Medical Park Pharmacy	METAXALONE	800 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (60760-289-30)
60760-289-60	60760-289	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200424	N/A	ANDA	ANDA204770	St. Mary's Medical Park Pharmacy	METAXALONE	800 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (60760-289-60)
60760-289-90	60760-289	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200331	N/A	ANDA	ANDA204770	St. Mary's Medical Park Pharmacy	METAXALONE	800 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (60760-289-90)
51655-792-20	51655-792	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20220120	N/A	ANDA	ANDA204770	Northwind Health Company, LLC	METAXALONE	800 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (51655-792-20)
51655-792-52	51655-792	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20220120	N/A	ANDA	ANDA204770	Northwind Health Company, LLC	METAXALONE	800 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-792-52)
51655-792-53	51655-792	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20220120	N/A	ANDA	ANDA204770	Northwind Health Company, LLC	METAXALONE	800 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (51655-792-53)