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
51224-206-30	51224-206	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20130923	20271130	ANDA	ANDA075274	TAGI Pharma Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (51224-206-30)
51224-206-50	51224-206	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20130923	20271130	ANDA	ANDA075274	TAGI Pharma Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51224-206-50)
68094-853-61	68094-853	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240815	N/A	ANDA	ANDA075274	Precision Dose Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	10 BLISTER PACK in 1 CARTON (68094-853-61) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59)
68094-853-62	68094-853	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20141029	20261231	ANDA	ANDA075274	Precision Dose Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	3 BLISTER PACK in 1 CARTON (68094-853-62) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59)
68094-853-66	68094-853	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240815	N/A	ANDA	ANDA075274	Precision Dose Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	2 BLISTER PACK in 1 CARTON (68094-853-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68094-853-59)
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)
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)
72162-1566-1	72162-1566	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20230912	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-1566-1)
72162-1566-3	72162-1566	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20230912	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-1566-3)
64850-300-01	64850-300	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20250815	N/A	ANDA	ANDA075274	Elite Laboratories, Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (64850-300-01)
64850-300-30	64850-300	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20250815	N/A	ANDA	ANDA075274	Elite Laboratories, Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (64850-300-30)
42291-632-30	42291-632	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20150326	20280630	ANDA	ANDA075274	AvKARE	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42291-632-30)
42291-632-60	42291-632	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20250724	20280630	ANDA	ANDA075274	AvKARE	NALTREXONE HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (42291-632-60)
71335-2419-1	71335-2419	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2419-1)
71335-2419-2	71335-2419	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2419-2)
71335-2419-3	71335-2419	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2419-3)
71335-2419-4	71335-2419	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71335-2419-4)
71335-2419-5	71335-2419	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2419-5)
71335-2419-6	71335-2419	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-2419-6)
71335-2419-7	71335-2419	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA075274	Bryant Ranch Prepack	NALTREXONE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2419-7)