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
50090-5789-4	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	15 TABLET, FILM COATED in 1 BOTTLE (50090-5789-4)
50090-5789-5	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	60 TABLET, FILM COATED in 1 BOTTLE (50090-5789-5)
50090-5789-9	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	120 TABLET, FILM COATED in 1 BOTTLE (50090-5789-9)
80425-0548-2	80425-0548	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250827	N/A	ANDA	ANDA211825	Advanced Rx of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-2)
80425-0548-3	80425-0548	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250827	N/A	ANDA	ANDA211825	Advanced Rx of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-3)
80425-0548-4	80425-0548	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, FILM COATED	ORAL	20250827	N/A	ANDA	ANDA211825	Advanced Rx of Tennessee, LLC	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0548-4)