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
68071-2831-2	68071-2831	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20220914	N/A	ANDA	ANDA077184	NuCare Pharmaceuticals,Inc.	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68071-2831-2)
71335-0151-3	71335-0151	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20200304	N/A	ANDA	ANDA077184	Bryant Ranch Prepack	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0151-3)
71335-0151-5	71335-0151	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20191008	N/A	ANDA	ANDA077184	Bryant Ranch Prepack	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0151-5)
71335-0151-6	71335-0151	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20220120	N/A	ANDA	ANDA077184	Bryant Ranch Prepack	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-0151-6)
71335-0151-7	71335-0151	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20220120	N/A	ANDA	ANDA077184	Bryant Ranch Prepack	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-0151-7)
71335-0151-8	71335-0151	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20210707	N/A	ANDA	ANDA077184	Bryant Ranch Prepack	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-0151-8)
71335-0151-2	71335-0151	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20191217	N/A	ANDA	ANDA077184	Bryant Ranch Prepack	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0151-2)
71335-0151-1	71335-0151	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20191018	N/A	ANDA	ANDA077184	Bryant Ranch Prepack	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0151-1)
57664-537-88	57664-537	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20051216	N/A	ANDA	ANDA077184	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (57664-537-88)
71335-0151-4	71335-0151	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20200121	N/A	ANDA	ANDA077184	Bryant Ranch Prepack	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0151-4)
57664-537-13	57664-537	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20051216	N/A	ANDA	ANDA077184	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (57664-537-13)
57664-537-18	57664-537	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TRAMADOL HYDROCHLORIDE AND ACETAMINOPHEN	TABLET, FILM COATED	ORAL	20051216	N/A	ANDA	ANDA077184	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (57664-537-18)