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
72888-163-05	72888-163	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230724	N/A	ANDA	ANDA208708	Advagen Pharma Limited	TRAMADOL HYDROCHLORIDE	75 mg/1	500 TABLET, COATED in 1 BOTTLE (72888-163-05)
72888-163-30	72888-163	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230724	N/A	ANDA	ANDA208708	Advagen Pharma Limited	TRAMADOL HYDROCHLORIDE	75 mg/1	30 TABLET, COATED in 1 BOTTLE (72888-163-30)
70518-3824-0	70518-3824	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230807	N/A	ANDA	ANDA208708	REMEDYREPACK INC.	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, COATED in 1 BLISTER PACK (70518-3824-0)
70518-3824-1	70518-3824	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230808	N/A	ANDA	ANDA208708	REMEDYREPACK INC.	TRAMADOL HYDROCHLORIDE	50 mg/1	60 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-1)
70518-3824-2	70518-3824	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230818	N/A	ANDA	ANDA208708	REMEDYREPACK INC.	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-2)
70518-3824-3	70518-3824	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230818	N/A	ANDA	ANDA208708	REMEDYREPACK INC.	TRAMADOL HYDROCHLORIDE	50 mg/1	180 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-3)
70518-3824-4	70518-3824	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20230831	N/A	ANDA	ANDA208708	REMEDYREPACK INC.	TRAMADOL HYDROCHLORIDE	50 mg/1	120 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3824-4)