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
63629-1905-1	63629-1905	HUMAN PRESCRIPTION DRUG	Methadone Hydrochloride	Methadone Hydrochloride	TABLET	ORAL	20211221	N/A	ANDA	ANDA211228	Bryant Ranch Prepack	METHADONE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (63629-1905-1)
63629-1906-1	63629-1906	HUMAN PRESCRIPTION DRUG	Methadone Hydrochloride	Methadone Hydrochloride	TABLET	ORAL	20211221	N/A	ANDA	ANDA211228	Bryant Ranch Prepack	METHADONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (63629-1906-1)
72865-120-01	72865-120	HUMAN PRESCRIPTION DRUG	Methadone Hydrochloride	Methadone Hydrochloride	TABLET	ORAL	20190103	N/A	ANDA	ANDA211228	XLCare Pharmaceuticals, Inc	METHADONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (72865-120-01)
72865-121-01	72865-121	HUMAN PRESCRIPTION DRUG	Methadone Hydrochloride	Methadone Hydrochloride	TABLET	ORAL	20190103	N/A	ANDA	ANDA211228	XLCare Pharmaceuticals, Inc	METHADONE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (72865-121-01)
31722-946-01	31722-946	HUMAN PRESCRIPTION DRUG	Methadone Hydrochloride	Methadone Hydrochloride	TABLET	ORAL	20190103	N/A	ANDA	ANDA211228	Camber Pharmaceuticals, Inc	METHADONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (31722-946-01)
31722-947-01	31722-947	HUMAN PRESCRIPTION DRUG	Methadone Hydrochloride	Methadone Hydrochloride	TABLET	ORAL	20190103	N/A	ANDA	ANDA211228	Camber Pharmaceuticals, Inc	METHADONE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (31722-947-01)