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
62756-460-64	62756-460	HUMAN PRESCRIPTION DRUG	Buprenorphine	Buprenorphine	TABLET	SUBLINGUAL	20160217	N/A	ANDA	ANDA201760	Sun Pharmaceutical Industries, Inc.	BUPRENORPHINE HYDROCHLORIDE	8 mg/1	3 BLISTER PACK in 1 CARTON (62756-460-64) / 10 TABLET in 1 BLISTER PACK
62756-460-83	62756-460	HUMAN PRESCRIPTION DRUG	Buprenorphine	Buprenorphine	TABLET	SUBLINGUAL	20160217	N/A	ANDA	ANDA201760	Sun Pharmaceutical Industries, Inc.	BUPRENORPHINE HYDROCHLORIDE	8 mg/1	30 TABLET in 1 BOTTLE (62756-460-83)
67296-1506-3	67296-1506	HUMAN PRESCRIPTION DRUG	Buprenorphine	Buprenorphine	TABLET	SUBLINGUAL	20160217	N/A	ANDA	ANDA201760	RedPharm Drug, Inc.	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	30 TABLET in 1 BOTTLE (67296-1506-3)
62756-459-83	62756-459	HUMAN PRESCRIPTION DRUG	Buprenorphine	Buprenorphine	TABLET	SUBLINGUAL	20160217	N/A	ANDA	ANDA201760	Sun Pharmaceutical Industries, Inc.	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	30 TABLET in 1 BOTTLE (62756-459-83)
62756-459-64	62756-459	HUMAN PRESCRIPTION DRUG	Buprenorphine	Buprenorphine	TABLET	SUBLINGUAL	20160217	N/A	ANDA	ANDA201760	Sun Pharmaceutical Industries, Inc.	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	3 BLISTER PACK in 1 CARTON (62756-459-64) / 10 TABLET in 1 BLISTER PACK
50268-129-15	50268-129	HUMAN PRESCRIPTION DRUG	Buprenorphine	Buprenorphine	TABLET	SUBLINGUAL	20240319	N/A	ANDA	ANDA201760	AvPAK	BUPRENORPHINE HYDROCHLORIDE	8 mg/1	50 BLISTER PACK in 1 BOX (50268-129-15) / 1 TABLET in 1 BLISTER PACK (50268-129-11)
50268-128-15	50268-128	HUMAN PRESCRIPTION DRUG	Buprenorphine	Buprenorphine	TABLET	SUBLINGUAL	20240319	N/A	ANDA	ANDA201760	AvPAK	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	50 BLISTER PACK in 1 BOX (50268-128-15) / 1 TABLET in 1 BLISTER PACK (50268-128-11)