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
76420-983-03	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)
76420-983-30	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	30 TABLET in 1 BOTTLE (76420-983-30)