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
29300-355-10	29300-355	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20191104	N/A	ANDA	ANDA211825	Unichem Pharmaceuticals (USA), Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (29300-355-10)
68788-4040-6	68788-4040	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-6)
68788-4040-1	68788-4040	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-1)
68788-4040-7	68788-4040	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-7)
68788-4040-8	68788-4040	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-8)
68788-4040-9	68788-4040	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA211825	Preferred Pharmaceuticals Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-9)