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
33342-269-07	33342-269	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA209404	Macleods Pharmaceuticals Limited	TRAMADOL HYDROCHLORIDE	100 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-269-07)
33342-269-10	33342-269	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA209404	Macleods Pharmaceuticals Limited	TRAMADOL HYDROCHLORIDE	100 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-269-10)
33342-269-11	33342-269	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA209404	Macleods Pharmaceuticals Limited	TRAMADOL HYDROCHLORIDE	100 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-269-11)
33342-270-07	33342-270	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA209404	Macleods Pharmaceuticals Limited	TRAMADOL HYDROCHLORIDE	200 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-270-07)
33342-270-10	33342-270	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA209404	Macleods Pharmaceuticals Limited	TRAMADOL HYDROCHLORIDE	200 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-270-10)
33342-270-11	33342-270	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA209404	Macleods Pharmaceuticals Limited	TRAMADOL HYDROCHLORIDE	200 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-270-11)
33342-271-07	33342-271	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA209404	Macleods Pharmaceuticals Limited	TRAMADOL HYDROCHLORIDE	300 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-271-07)
33342-271-10	33342-271	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA209404	Macleods Pharmaceuticals Limited	TRAMADOL HYDROCHLORIDE	300 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-271-10)
33342-271-11	33342-271	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20250131	N/A	ANDA	ANDA209404	Macleods Pharmaceuticals Limited	TRAMADOL HYDROCHLORIDE	300 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (33342-271-11)