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
60687-626-65	60687-626	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20220310	N/A	ANDA	ANDA205601	American Health Packaging	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	2 mg/1; .5 mg/1	50 BLISTER PACK in 1 CARTON (60687-626-65) / 1 TABLET in 1 BLISTER PACK (60687-626-11)
60687-637-65	60687-637	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20220314	N/A	ANDA	ANDA205601	American Health Packaging	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	8 mg/1; 2 mg/1	50 BLISTER PACK in 1 CARTON (60687-637-65) / 1 TABLET in 1 BLISTER PACK (60687-637-11)
72162-1346-3	72162-1346	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20240312	N/A	ANDA	ANDA205601	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	2 mg/1; .5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72162-1346-3)
72162-1347-3	72162-1347	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20240312	N/A	ANDA	ANDA205601	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	8 mg/1; 2 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72162-1347-3)
63629-9482-1	63629-9482	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20221212	N/A	ANDA	ANDA205601	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	2 mg/1; .5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (63629-9482-1)
63629-9483-1	63629-9483	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20221212	N/A	ANDA	ANDA205601	Bryant Ranch Prepack	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	8 mg/1; 2 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (63629-9483-1)
70518-3389-0	70518-3389	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20220316	N/A	ANDA	ANDA205601	REMEDYREPACK INC.	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	8 mg/1; 2 mg/1	30 TABLET in 1 BLISTER PACK (70518-3389-0)
42858-601-03	42858-601	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20200413	N/A	ANDA	ANDA205601	Rhodes Pharmaceuticals L.P.	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	2 mg/1; .5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (42858-601-03)
42858-602-03	42858-602	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20200413	N/A	ANDA	ANDA205601	Rhodes Pharmaceuticals L.P.	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	8 mg/1; 2 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (42858-602-03)
70518-3487-0	70518-3487	HUMAN PRESCRIPTION DRUG	Buprenorphine and Naloxone	Buprenorphine and Naloxone	TABLET	SUBLINGUAL	20220819	N/A	ANDA	ANDA205601	REMEDYREPACK INC.	BUPRENORPHINE HYDROCHLORIDE; NALOXONE HYDROCHLORIDE DIHYDRATE	2 mg/1; .5 mg/1	30 TABLET in 1 BLISTER PACK (70518-3487-0)