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
68094-853-62	68094-853	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20141029	N/A	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)
68094-909-50	68094-909	HUMAN PRESCRIPTION DRUG	Naltrexone Hydrochloride	Naltrexone Hydrochloride	TABLET, FILM COATED	ORAL	20240215	N/A	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	N/A	ANDA	ANDA075274	Precision Dose Inc.	NALTREXONE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68094-909-30)