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
72162-1346-3	72162-1346	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20260403	N/A	ANDA	ANDA205601	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	2 mg/1; .5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72162-1346-3)
71335-2828-1	71335-2828	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20251023	N/A	ANDA	ANDA205601	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	8 mg/1; 2 mg/1	30 TABLET in 1 BOTTLE (71335-2828-1)
63629-9483-1	63629-9483	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20221212	N/A	ANDA	ANDA205601	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	8 mg/1; 2 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (63629-9483-1)