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
76420-244-30	76420-244	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220725	N/A	ANDA	ANDA201384	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-30)
76420-244-60	76420-244	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220725	N/A	ANDA	ANDA201384	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-60)
76420-244-90	76420-244	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220725	N/A	ANDA	ANDA201384	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-244-90)
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)
71205-708-30	71205-708	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20221031	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	200 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-30)
71205-708-60	71205-708	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20221031	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	200 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-60)
71205-708-90	71205-708	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20221031	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	200 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-708-90)
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)
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)
47335-859-83	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)
47335-859-88	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)
63629-8324-1	63629-8324	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20200622	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8324-1)
63629-8324-2	63629-8324	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20211004	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8324-2)
63629-8324-3	63629-8324	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8324-3)
63629-8324-4	63629-8324	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20240403	N/A	ANDA	ANDA201384	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	300 mg/1	120 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8324-4)
71205-656-60	71205-656	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220427	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	300 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-656-60)
71205-656-90	71205-656	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220427	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-656-90)