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
61919-073-21	61919-073	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, COATED	ORAL	20180615	N/A	ANDA	ANDA076003	DIRECT RX	TRAMADOL HYDROCHLORIDE	50 mg/1	21 TABLET, COATED in 1 BOTTLE (61919-073-21)
68084-808-01	68084-808	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20140805	20250731	ANDA	ANDA076003	American Health Packaging	TRAMADOL HYDROCHLORIDE	50 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-808-01) / 1 TABLET, COATED in 1 BLISTER PACK (68084-808-11)
60687-795-01	60687-795	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET, COATED	ORAL	20240120	N/A	ANDA	ANDA076003	American Health Packaging	TRAMADOL HYDROCHLORIDE	50 mg/1	100 BLISTER PACK in 1 CARTON (60687-795-01) / 1 TABLET, COATED in 1 BLISTER PACK (60687-795-11)