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
31722-480-30	31722-480	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	buprenorphine and naloxone	FILM, SOLUBLE	BUCCAL; SUBLINGUAL	20260501	N/A	ANDA	ANDA219850	Camber Pharmaceuticals, Inc.	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE	4 mg/1; 1 mg/1	30 POUCH in 1 CARTON (31722-480-30) / 1 FILM, SOLUBLE in 1 POUCH (31722-480-31)
31722-482-30	31722-482	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	buprenorphine and naloxone	FILM, SOLUBLE	BUCCAL; SUBLINGUAL	20260501	N/A	ANDA	ANDA219850	Camber Pharmaceuticals, Inc.	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE	12 mg/1; 3 mg/1	30 POUCH in 1 CARTON (31722-482-30) / 1 FILM, SOLUBLE in 1 POUCH (31722-482-31)
31722-479-30	31722-479	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	buprenorphine and naloxone	FILM, SOLUBLE	BUCCAL; SUBLINGUAL	20260501	N/A	ANDA	ANDA219850	Camber Pharmaceuticals, Inc.	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE	2 mg/1; .5 mg/1	30 POUCH in 1 CARTON (31722-479-30) / 1 FILM, SOLUBLE in 1 POUCH (31722-479-31)
31722-481-30	31722-481	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	buprenorphine and naloxone	FILM, SOLUBLE	BUCCAL; SUBLINGUAL	20260501	N/A	ANDA	ANDA219850	Camber Pharmaceuticals, Inc.	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE	8 mg/1; 2 mg/1	30 POUCH in 1 CARTON (31722-481-30) / 1 FILM, SOLUBLE in 1 POUCH (31722-481-31)