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
17856-3556-5	17856-3556	HUMAN PRESCRIPTION DRUG	Methadone Hydrochloride	Methadone Hydrochloride	SOLUTION	ORAL	20200427	N/A	ANDA	ANDA087997	ATLANTIC BIOLOGICALS CORP.	METHADONE HYDROCHLORIDE	10 mg/5mL	72 CUP in 1 CASE (17856-3556-5) / 10 mL in 1 CUP
17856-3556-6	17856-3556	HUMAN PRESCRIPTION DRUG	Methadone Hydrochloride	Methadone Hydrochloride	SOLUTION	ORAL	20200427	N/A	ANDA	ANDA087997	ATLANTIC BIOLOGICALS CORP.	METHADONE HYDROCHLORIDE	10 mg/5mL	72 CUP, UNIT-DOSE in 1 CASE (17856-3556-6) / 5 mL in 1 CUP, UNIT-DOSE
0054-3556-63	0054-3556	HUMAN PRESCRIPTION DRUG	Methadone Hydrochloride	Methadone Hydrochloride	SOLUTION	ORAL	19820830	N/A	ANDA	ANDA087997	Hikma Pharmaceuticals USA Inc.	METHADONE HYDROCHLORIDE	10 mg/5mL	500 mL in 1 BOTTLE (0054-3556-63)