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
71335-2481-1	71335-2481	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240827	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2481-1)
70518-4344-0	70518-4344	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20250520	N/A	ANDA	ANDA075274	REMEDYREPACK INC.	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4344-0)
72162-2311-1	72162-2311	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240513	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-2311-1)
72162-2311-3	72162-2311	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240513	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-2311-3)
71335-2743-1	71335-2743	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20250729	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2743-1)
68071-3654-3	68071-3654	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240724	N/A	ANDA	ANDA075274	NuCare Pharmaceuticals Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3654-3)
72162-2529-1	72162-2529	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20250903	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-2529-1)
72162-2529-3	72162-2529	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20250903	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-2529-3)
71335-2987-1	71335-2987	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20251110	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2987-1)
71335-3011-1	71335-3011	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20251118	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-3011-1)
71335-3012-1	71335-3012	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20251118	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-3012-1)
71335-3039-1	71335-3039	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20251203	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-3039-1)
71335-3040-1	71335-3040	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20251203	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-3040-1)
71335-2480-1	71335-2480	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240827	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2480-1)
68094-909-50	68094-909	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240215	20280630	ANDA	ANDA075274	Precision Dose Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68094-909-50)
68094-909-30	68094-909	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240215	20280630	ANDA	ANDA075274	Precision Dose Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68094-909-30)