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
68788-4035-1	68788-4035	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250929	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-1)
68788-4035-2	68788-4035	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250929	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-2)
68788-4035-3	68788-4035	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250929	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-3)
68788-4035-4	68788-4035	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250929	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-4)
68788-4035-5	68788-4035	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250929	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-5)
68788-4035-6	68788-4035	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250929	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-6)
68788-4035-7	68788-4035	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250929	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-7)
68788-4035-8	68788-4035	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250929	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-8)
68788-4035-9	68788-4035	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250929	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-9)
87063-117-01	87063-117	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20260216	N/A	ANDA	ANDA211825	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-01)
87063-117-05	87063-117	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20260216	N/A	ANDA	ANDA211825	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-05)
87063-117-10	87063-117	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20260216	N/A	ANDA	ANDA211825	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-10)
87063-117-20	87063-117	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20260216	N/A	ANDA	ANDA211825	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-20)
87063-117-30	87063-117	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20260216	N/A	ANDA	ANDA211825	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-30)
87063-117-50	87063-117	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20260216	N/A	ANDA	ANDA211825	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-50)
87063-117-60	87063-117	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20260216	N/A	ANDA	ANDA211825	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-60)
87063-117-90	87063-117	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20260216	N/A	ANDA	ANDA211825	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-90)
50090-5790-1	50090-5790	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20220208	N/A	ANDA	ANDA211825	A-S Medication Solutions	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5790-1)
50090-5790-2	50090-5790	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20211008	N/A	ANDA	ANDA211825	A-S Medication Solutions	TRAMADOL HYDROCHLORIDE	50 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (50090-5790-2)
50090-5789-0	50090-5789	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20211008	N/A	ANDA	ANDA211825	A-S Medication Solutions	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-5789-0)