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
62135-242-90	62135-242	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20220105	N/A	ANDA	ANDA207905	Chartwell RX, LLC	NALTREXONE HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62135-242-90)
62135-242-60	62135-242	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240611	N/A	ANDA	ANDA207905	Chartwell RX, LLC	NALTREXONE HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62135-242-60)
62135-242-30	62135-242	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20220105	N/A	ANDA	ANDA207905	Chartwell RX, LLC	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62135-242-30)
23155-886-01	23155-886	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20231006	N/A	ANDA	ANDA207905	Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (23155-886-01)
23155-886-03	23155-886	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20231006	N/A	ANDA	ANDA207905	Heritage Pharmaceuticals Inc d/b/a Avet Pharmaceuticals Inc	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (23155-886-03)