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
80425-0127-1	80425-0127	HUMAN PRESCRIPTION DRUG	Tramadol HCL ER	Tramadol HCL	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Advanced Rx Pharmacy of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0127-1)
80425-0127-2	80425-0127	HUMAN PRESCRIPTION DRUG	Tramadol HCL ER	Tramadol HCL	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Advanced Rx Pharmacy of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	200 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0127-2)
47335-531-08	47335-531	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-531-08)
47335-531-18	47335-531	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-531-18)
47335-531-83	47335-531	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-531-83)
47335-531-88	47335-531	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-531-88)
47335-537-08	47335-537	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-537-08)
47335-537-18	47335-537	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	300 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-537-18)
47335-537-83	47335-537	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-537-83)
47335-537-88	47335-537	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-537-88)
47335-533-08	47335-533	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-533-08)
47335-533-18	47335-533	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	200 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-533-18)
47335-533-83	47335-533	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-533-83)
47335-533-88	47335-533	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111230	N/A	ANDA	ANDA091607	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-533-88)