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
76420-246-30	76420-246	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220725	N/A	ANDA	ANDA201384	Asclemed USA, Inc.	TRAMADOL HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (76420-246-30)
47335-859-08	47335-859	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-08)
47335-859-18	47335-859	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-18)
47335-859-83	47335-859	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-83)
47335-859-88	47335-859	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20111212	N/A	ANDA	ANDA201384	Sun Pharmaceutical Industries, Inc.	TRAMADOL HYDROCHLORIDE	100 mg/1	100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-859-88)