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
64980-614-01	64980-614	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET	ORAL	20240805	N/A	ANDA	ANDA075968	Rising Pharma Holdings, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (64980-614-01)
64980-614-10	64980-614	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET	ORAL	20240805	N/A	ANDA	ANDA075968	Rising Pharma Holdings, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	1000 TABLET in 1 BOTTLE (64980-614-10)
64980-614-50	64980-614	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET	ORAL	20240805	N/A	ANDA	ANDA075968	Rising Pharma Holdings, Inc.	TRAMADOL HYDROCHLORIDE	50 mg/1	500 TABLET in 1 BOTTLE (64980-614-50)
64980-663-01	64980-663	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET	ORAL	20241024	N/A	ANDA	ANDA075968	Rising Pharma Holdings, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (64980-663-01)
60760-727-20	60760-727	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET	ORAL	20251113	N/A	ANDA	ANDA075968	ST. MARY'S MEDICAL PARK PHARMACY	TRAMADOL HYDROCHLORIDE	50 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (60760-727-20)
60760-727-30	60760-727	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET	ORAL	20251105	N/A	ANDA	ANDA075968	ST. MARY'S MEDICAL PARK PHARMACY	TRAMADOL HYDROCHLORIDE	50 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (60760-727-30)
60760-727-50	60760-727	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET	ORAL	20251105	N/A	ANDA	ANDA075968	ST. MARY'S MEDICAL PARK PHARMACY	TRAMADOL HYDROCHLORIDE	50 mg/1	50 TABLET in 1 BOTTLE, PLASTIC (60760-727-50)
60760-727-90	60760-727	HUMAN PRESCRIPTION DRUG	Tramadol Hydrochloride	Tramadol Hydrochloride	TABLET	ORAL	20251105	N/A	ANDA	ANDA075968	ST. MARY'S MEDICAL PARK PHARMACY	TRAMADOL HYDROCHLORIDE	50 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (60760-727-90)