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
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)
80425-0524-3	80425-0524	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20250529	N/A	ANDA	ANDA207466	Advanced Rx of Tennessee, LLC	METAXALONE	800 mg/1	90 TABLET in 1 BOTTLE (80425-0524-3)
80425-0524-1	80425-0524	HUMAN PRESCRIPTION DRUG	Metaxalone	Metaxalone	TABLET	ORAL	20250529	N/A	ANDA	ANDA207466	Advanced Rx of Tennessee, LLC	METAXALONE	800 mg/1	30 TABLET in 1 BOTTLE (80425-0524-1)
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)