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
71335-2981-7	71335-2981	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20251126	N/A	ANDA	ANDA205601	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	8 mg/1; 2 mg/1	6 TABLET in 1 BOTTLE, PLASTIC (71335-2981-7)
71335-2981-8	71335-2981	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20251126	N/A	ANDA	ANDA205601	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	8 mg/1; 2 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (71335-2981-8)
71335-2981-9	71335-2981	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20251126	N/A	ANDA	ANDA205601	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	8 mg/1; 2 mg/1	21 TABLET in 1 BOTTLE, PLASTIC (71335-2981-9)