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
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)
47335-861-08	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)
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)
47335-859-83	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)
47335-859-18	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	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-18)
47335-859-08	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 (47335-859-08)
50090-6033-0	50090-6033	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220712	N/A	ANDA	ANDA201384	A-S Medication Solutions	TRAMADOL HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6033-0)
71335-1675-4	71335-1675	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	100 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1675-4)
71335-1676-1	71335-1676	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200710	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-1)
71335-1676-2	71335-1676	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200708	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	200 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-2)
71335-1676-3	71335-1676	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200813	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	200 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-3)
71335-1676-4	71335-1676	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20240404	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	200 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1676-4)
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)