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
76420-983-02	76420-983	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride and Acetaminophen	Tramadol Hydrochloride and Acetaminophen	TABLET	ORAL	20220114	N/A	ANDA	ANDA090485	Asclemed USA, Inc.	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	2 TABLET in 1 BOTTLE (76420-983-02)
76420-983-03	76420-983	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride and Acetaminophen	Tramadol Hydrochloride and Acetaminophen	TABLET	ORAL	20220114	N/A	ANDA	ANDA090485	Asclemed USA, Inc.	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	3 TABLET in 1 BOTTLE (76420-983-03)
76420-983-10	76420-983	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride and Acetaminophen	Tramadol Hydrochloride and Acetaminophen	TABLET	ORAL	20220114	N/A	ANDA	ANDA090485	Asclemed USA, Inc.	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	10 TABLET in 1 BOTTLE (76420-983-10)
50268-774-15	50268-774	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride and Acetaminophen	Tramadol Hydrochloride and Acetaminophen	TABLET	ORAL	20150114	20270331	ANDA	ANDA090485	AvPAK	ACETAMINOPHEN; TRAMADOL HYDROCHLORIDE	325 mg/1; 37.5 mg/1	50 BLISTER PACK in 1 BOX (50268-774-15) / 1 TABLET in 1 BLISTER PACK (50268-774-11)