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
68071-2952-5	68071-2952	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20230328	N/A	ANDA	ANDA203494	NuCare Pharmaceuticals,Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (68071-2952-5)
68071-2952-9	68071-2952	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20230328	N/A	ANDA	ANDA203494	NuCare Pharmaceuticals,Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-2952-9)
68071-2952-6	68071-2952	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20230328	N/A	ANDA	ANDA203494	NuCare Pharmaceuticals,Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-2952-6)
68071-2952-8	68071-2952	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20230328	N/A	ANDA	ANDA203494	NuCare Pharmaceuticals,Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (68071-2952-8)
68071-2952-3	68071-2952	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20230328	N/A	ANDA	ANDA203494	NuCare Pharmaceuticals,Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-2952-3)
16571-716-50	16571-716	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20200923	N/A	ANDA	ANDA203494	Rising Pharma Holdings, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (16571-716-50)
16571-716-01	16571-716	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20200923	N/A	ANDA	ANDA203494	Rising Pharma Holdings, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (16571-716-01)
16571-716-10	16571-716	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20200923	N/A	ANDA	ANDA203494	Rising Pharma Holdings, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (16571-716-10)
70518-3586-1	70518-3586	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20240301	N/A	ANDA	ANDA203494	REMEDYREPACK INC.	TRAMADOL HYDROCHLORIDE	50 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3586-1)