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
10702-071-01	10702-071	HUMAN PRESCRIPTION DRUG	Oxymorphone Hydrochloride	Oxymorphone Hydrochloride	TABLET	ORAL	20130211	N/A	ANDA	ANDA203601	KVK-Tech, Inc.	OXYMORPHONE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (10702-071-01)
10702-071-06	10702-071	HUMAN PRESCRIPTION DRUG	Oxymorphone Hydrochloride	Oxymorphone Hydrochloride	TABLET	ORAL	20180625	N/A	ANDA	ANDA203601	KVK-Tech, Inc.	OXYMORPHONE HYDROCHLORIDE	10 mg/1	60 TABLET in 1 BOTTLE (10702-071-06)
10702-070-01	10702-070	HUMAN PRESCRIPTION DRUG	Oxymorphone Hydrochloride	Oxymorphone Hydrochloride	TABLET	ORAL	20130211	N/A	ANDA	ANDA203601	KVK-Tech, Inc.	OXYMORPHONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (10702-070-01)
10702-070-06	10702-070	HUMAN PRESCRIPTION DRUG	Oxymorphone Hydrochloride	Oxymorphone Hydrochloride	TABLET	ORAL	20180625	N/A	ANDA	ANDA203601	KVK-Tech, Inc.	OXYMORPHONE HYDROCHLORIDE	5 mg/1	60 TABLET in 1 BOTTLE (10702-070-06)