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
71205-066-40	71205-066	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180702	N/A	ANDA	ANDA090404	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71205-066-40)
71205-066-60	71205-066	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180702	N/A	ANDA	ANDA090404	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-066-60)
71205-066-72	71205-066	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180702	N/A	ANDA	ANDA090404	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71205-066-72)
71205-066-78	71205-066	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180702	N/A	ANDA	ANDA090404	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71205-066-78)
71205-066-90	71205-066	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180702	N/A	ANDA	ANDA090404	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-066-90)
68382-319-01	68382-319	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20110131	N/A	ANDA	ANDA090404	Zydus Pharmaceuticals USA Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-319-01)
68382-319-05	68382-319	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20110131	N/A	ANDA	ANDA090404	Zydus Pharmaceuticals USA Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68382-319-05)
68382-319-10	68382-319	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20110131	N/A	ANDA	ANDA090404	Zydus Pharmaceuticals USA Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68382-319-10)
68382-319-77	68382-319	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20110131	N/A	ANDA	ANDA090404	Zydus Pharmaceuticals USA Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	100 BLISTER PACK in 1 CARTON (68382-319-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-319-30)
61919-597-20	61919-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA090404	DirectRX	TRAMADOL HYDROCHLORIDE	50 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (61919-597-20)
61919-597-30	61919-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA090404	DirectRX	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (61919-597-30)
61919-597-40	61919-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA090404	DirectRX	TRAMADOL HYDROCHLORIDE	50 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (61919-597-40)
61919-597-60	61919-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA090404	DirectRX	TRAMADOL HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (61919-597-60)
61919-597-72	61919-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA090404	DirectRX	TRAMADOL HYDROCHLORIDE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (61919-597-72)
61919-597-82	61919-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA090404	DirectRX	TRAMADOL HYDROCHLORIDE	50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (61919-597-82)
61919-597-84	61919-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA090404	DirectRX	TRAMADOL HYDROCHLORIDE	50 mg/1	240 TABLET, FILM COATED in 1 BOTTLE (61919-597-84)
61919-597-90	61919-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA090404	DirectRX	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (61919-597-90)
71205-066-30	71205-066	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180702	N/A	ANDA	ANDA090404	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-066-30)
71205-066-20	71205-066	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180702	N/A	ANDA	ANDA090404	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71205-066-20)
71205-066-15	71205-066	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, FILM COATED	ORAL	20180702	N/A	ANDA	ANDA090404	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	50 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71205-066-15)