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
80425-0141-1	80425-0141	HUMAN PRESCRIPTION DRUG	Tramadol HCL ER	Tramadol HCL	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Advanced Rx Pharmacy of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0141-1)
80425-0141-2	80425-0141	HUMAN PRESCRIPTION DRUG	Tramadol HCL ER	Tramadol HCL	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Advanced Rx Pharmacy of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0141-2)
80425-0141-3	80425-0141	HUMAN PRESCRIPTION DRUG	Tramadol HCL ER	Tramadol HCL	TABLET, EXTENDED RELEASE	ORAL	20241121	N/A	ANDA	ANDA201384	Advanced Rx Pharmacy of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	100 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0141-3)
47335-859-88	47335-859	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-88)
47335-860-08	47335-860	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-08)
47335-860-18	47335-860	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	200 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-18)
47335-860-83	47335-860	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-83)
47335-860-88	47335-860	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	200 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-88)
47335-861-18	47335-861	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	300 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-18)
47335-861-83	47335-861	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-83)
47335-861-88	47335-861	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-88)
47335-861-08	47335-861	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	300 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-861-08)
63187-597-30	63187-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-597-30)
63187-597-60	63187-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-597-60)
63187-597-90	63187-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	100 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-597-90)
61919-893-30	61919-893	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20150626	N/A	ANDA	ANDA201384	DIRECT RX	TRAMADOL HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-30)
61919-893-60	61919-893	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20140101	N/A	ANDA	ANDA201384	DIRECT RX	TRAMADOL HYDROCHLORIDE	200 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-893-60)
71335-1675-1	71335-1675	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200723	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1675-1)
71335-1675-2	71335-1675	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200722	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1675-2)
47335-859-83	47335-859	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-83)