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
71205-656-90	71205-656	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220427	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-656-90)
71205-656-30	71205-656	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20220427	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-656-30)
63187-597-30	63187-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-597-30)
63187-597-60	63187-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	100 mg/1	60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-597-60)
63187-597-90	63187-597	HUMAN PRESCRIPTION DRUG	TRAMADOL HYDROCHLORIDE	TRAMADOL HYDROCHLORIDE	TABLET, EXTENDED RELEASE	ORAL	20181201	N/A	ANDA	ANDA201384	Proficient Rx LP	TRAMADOL HYDROCHLORIDE	100 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63187-597-90)