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
71335-0950-8	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)
63629-9475-1	63629-9475	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20221128	N/A	ANDA	ANDA207276	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	30 TABLET in 1 BOTTLE (63629-9475-1)
72162-1345-3	72162-1345	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20240422	N/A	ANDA	ANDA207276	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE	8 mg/1	30 TABLET in 1 BOTTLE (72162-1345-3)
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)
58118-0501-8	58118-0501	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20171025	N/A	ANDA	ANDA207276	Clinical Solutions Wholesale, LLC	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	30 TABLET in 1 BLISTER PACK (58118-0501-8)
42858-502-03	42858-502	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20171025	N/A	ANDA	ANDA207276	Rhodes Pharmaceuticals L.P.	BUPRENORPHINE HYDROCHLORIDE	8 mg/1	30 TABLET in 1 BOTTLE (42858-502-03)
50090-5805-0	50090-5805	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20211015	N/A	ANDA	ANDA207276	A-S Medication Solutions	BUPRENORPHINE HYDROCHLORIDE	8 mg/1	30 TABLET in 1 BOTTLE (50090-5805-0)
42858-501-03	42858-501	HUMAN PRESCRIPTION DRUG	BUPRENORPHINE	BUPRENORPHINE	TABLET	SUBLINGUAL	20171025	N/A	ANDA	ANDA207276	Rhodes Pharmaceuticals L.P.	BUPRENORPHINE HYDROCHLORIDE	2 mg/1	30 TABLET in 1 BOTTLE (42858-501-03)