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
72189-311-90	72189-311	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, COATED	ORAL	20220112	N/A	ANDA	ANDA208708	DirectRx	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, COATED in 1 BOTTLE (72189-311-90)
72888-162-00	72888-162	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20231128	N/A	ANDA	ANDA208708	Advagen Pharma Limited	TRAMADOL HYDROCHLORIDE	25 mg/1	1000 TABLET, COATED in 1 BOTTLE (72888-162-00)
72888-162-01	72888-162	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20231128	N/A	ANDA	ANDA208708	Advagen Pharma Limited	TRAMADOL HYDROCHLORIDE	25 mg/1	100 TABLET, COATED in 1 BOTTLE (72888-162-01)
72888-162-05	72888-162	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20231128	N/A	ANDA	ANDA208708	Advagen Pharma Limited	TRAMADOL HYDROCHLORIDE	25 mg/1	500 TABLET, COATED in 1 BOTTLE (72888-162-05)
72888-162-30	72888-162	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20231128	N/A	ANDA	ANDA208708	Advagen Pharma Limited	TRAMADOL HYDROCHLORIDE	25 mg/1	30 TABLET, COATED in 1 BOTTLE (72888-162-30)
76420-734-30	76420-734	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240522	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	30 TABLET, COATED in 1 BOTTLE (76420-734-30)
76420-734-60	76420-734	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240522	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	60 TABLET, COATED in 1 BOTTLE (76420-734-60)
76420-734-90	76420-734	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240522	N/A	ANDA	ANDA208708	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	90 TABLET, COATED in 1 BOTTLE (76420-734-90)
68788-8121-8	68788-8121	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20220105	N/A	ANDA	ANDA208708	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	120 TABLET, COATED in 1 BOTTLE (68788-8121-8)
68788-8121-9	68788-8121	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20220105	N/A	ANDA	ANDA208708	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, COATED in 1 BOTTLE (68788-8121-9)
68788-8121-1	68788-8121	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20220105	N/A	ANDA	ANDA208708	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET, COATED in 1 BOTTLE (68788-8121-1)
68788-8121-2	68788-8121	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20220105	N/A	ANDA	ANDA208708	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	20 TABLET, COATED in 1 BOTTLE (68788-8121-2)
68788-8121-3	68788-8121	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20220105	N/A	ANDA	ANDA208708	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, COATED in 1 BOTTLE (68788-8121-3)
68788-8121-4	68788-8121	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20220105	N/A	ANDA	ANDA208708	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	40 TABLET, COATED in 1 BOTTLE (68788-8121-4)
68788-8121-5	68788-8121	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20220105	N/A	ANDA	ANDA208708	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	15 TABLET, COATED in 1 BOTTLE (68788-8121-5)