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
71335-2721-4	71335-2721	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20250926	N/A	ANDA	ANDA208708	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	50 mg/1	10 TABLET, COATED in 1 BOTTLE (71335-2721-4)
71335-2721-3	71335-2721	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20250926	N/A	ANDA	ANDA208708	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	50 mg/1	56 TABLET, COATED in 1 BOTTLE (71335-2721-3)
71335-2721-2	71335-2721	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20250926	N/A	ANDA	ANDA208708	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	50 mg/1	84 TABLET, COATED in 1 BOTTLE (71335-2721-2)
71335-2721-1	71335-2721	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20250926	N/A	ANDA	ANDA208708	Bryant Ranch Prepack	TRAMADOL HYDROCHLORIDE	50 mg/1	8 TABLET, COATED in 1 BOTTLE (71335-2721-1)
52817-196-00	52817-196	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20200224	N/A	ANDA	ANDA208708	TRUPHARMA LLC	TRAMADOL HYDROCHLORIDE	100 mg/1	1000 TABLET, COATED in 1 BOTTLE (52817-196-00)
52817-196-10	52817-196	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20200224	N/A	ANDA	ANDA208708	TRUPHARMA LLC	TRAMADOL HYDROCHLORIDE	100 mg/1	100 TABLET, COATED in 1 BOTTLE (52817-196-10)
52817-196-50	52817-196	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20200224	N/A	ANDA	ANDA208708	TRUPHARMA LLC	TRAMADOL HYDROCHLORIDE	100 mg/1	500 TABLET, COATED in 1 BOTTLE (52817-196-50)
52817-195-00	52817-195	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20200901	N/A	ANDA	ANDA208708	TRUPHARMA LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	1000 TABLET, COATED in 1 BOTTLE (52817-195-00)
52817-195-10	52817-195	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20200901	N/A	ANDA	ANDA208708	TRUPHARMA LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET, COATED in 1 BOTTLE (52817-195-10)
52817-195-50	52817-195	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20200901	N/A	ANDA	ANDA208708	TRUPHARMA LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	500 TABLET, COATED in 1 BOTTLE (52817-195-50)
76420-732-01	76420-732	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240522	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	25 mg/1	100 TABLET, COATED in 1 BOTTLE (76420-732-01)
76420-732-60	76420-732	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240522	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	25 mg/1	60 TABLET, COATED in 1 BOTTLE (76420-732-60)
76420-732-90	76420-732	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240522	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	25 mg/1	90 TABLET, COATED in 1 BOTTLE (76420-732-90)
76420-733-00	76420-733	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240522	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	1000 TABLET, COATED in 1 BOTTLE (76420-733-00)
76420-733-01	76420-733	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240522	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET, COATED in 1 BOTTLE (76420-733-01)
76420-733-02	76420-733	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20250814	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	2 TABLET, COATED in 1 BOTTLE (76420-733-02)
76420-733-05	76420-733	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240522	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	500 TABLET, COATED in 1 BOTTLE (76420-733-05)
76420-733-10	76420-733	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20250814	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	1 TABLET, COATED in 1 BOTTLE (76420-733-10)
76420-733-12	76420-733	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20250714	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	120 TABLET, COATED in 1 BOTTLE (76420-733-12)
76420-733-30	76420-733	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240522	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, COATED in 1 BOTTLE (76420-733-30)