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
71335-1320-3	71335-1320	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20190829	N/A	ANDA	ANDA208774	Bryant Ranch Prepack	METAXALONE	800 mg/1	90 TABLET in 1 BOTTLE (71335-1320-3)
51655-602-20	51655-602	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20210219	N/A	ANDA	ANDA208774	Northwind Pharmaceuticals	METAXALONE	800 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (51655-602-20)
72789-122-30	72789-122	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200925	N/A	ANDA	ANDA208774	PD-Rx Pharmaceuticals, Inc.	METAXALONE	800 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (72789-122-30)
71205-470-30	71205-470	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200824	N/A	ANDA	ANDA208774	Proficient Rx LP	METAXALONE	800 mg/1	30 TABLET in 1 BOTTLE (71205-470-30)
71205-470-60	71205-470	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200824	N/A	ANDA	ANDA208774	Proficient Rx LP	METAXALONE	800 mg/1	60 TABLET in 1 BOTTLE (71205-470-60)
71205-470-90	71205-470	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200824	N/A	ANDA	ANDA208774	Proficient Rx LP	METAXALONE	800 mg/1	90 TABLET in 1 BOTTLE (71205-470-90)
71205-961-55	71205-961	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200731	20240630	ANDA	ANDA208774	Proficient Rx LP	METAXALONE	800 mg/1	500 TABLET in 1 BOTTLE (71205-961-55)
72162-1808-1	72162-1808	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20231006	N/A	ANDA	ANDA208774	Bryant Ranch Prepack	METAXALONE	800 mg/1	100 TABLET in 1 BOTTLE (72162-1808-1)
71205-961-30	71205-961	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20200731	20240630	ANDA	ANDA208774	Proficient Rx LP	METAXALONE	800 mg/1	30 TABLET in 1 BOTTLE (71205-961-30)