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
71335-0950-1	71335-0950	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20180913	N/A	ANDA	ANDA207276	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	60 TABLET in 1 BOTTLE (71335-0950-1)
71335-0950-2	71335-0950	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20180913	N/A	ANDA	ANDA207276	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	90 TABLET in 1 BOTTLE (71335-0950-2)
71335-0950-3	71335-0950	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20220923	N/A	ANDA	ANDA207276	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	30 TABLET in 1 BOTTLE (71335-0950-3)
71335-0950-4	71335-0950	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20220923	N/A	ANDA	ANDA207276	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	7 TABLET in 1 BOTTLE (71335-0950-4)
71335-0950-5	71335-0950	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20220923	N/A	ANDA	ANDA207276	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	28 TABLET in 1 BOTTLE (71335-0950-5)
71335-0950-6	71335-0950	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20220923	N/A	ANDA	ANDA207276	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	1 TABLET in 1 BOTTLE (71335-0950-6)
71335-0950-7	71335-0950	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20220923	N/A	ANDA	ANDA207276	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	12 TABLET in 1 BOTTLE (71335-0950-7)
71335-0950-8	71335-0950	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20220923	N/A	ANDA	ANDA207276	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	120 TABLET in 1 BOTTLE (71335-0950-8)
60687-481-21	60687-481	HUMAN PRESCRIPTION DRUG	Buprenorphine	Buprenorphine	TABLET	SUBLINGUAL	20200206	N/A	ANDA	ANDA207276	American Health Packaging	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-481-21) / 1 TABLET in 1 BLISTER PACK (60687-481-11)