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
13107-104-01	13107-104	HUMAN PRESCRIPTION DRUG	Oxymorphone Hydrochloride	Oxymorphone Hydrochloride	TABLET	ORAL	20160426	N/A	ANDA	ANDA204459	Aurolife Pharma, LLC	OXYMORPHONE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (13107-104-01)
13107-104-30	13107-104	HUMAN PRESCRIPTION DRUG	Oxymorphone Hydrochloride	Oxymorphone Hydrochloride	TABLET	ORAL	20160426	N/A	ANDA	ANDA204459	Aurolife Pharma, LLC	OXYMORPHONE HYDROCHLORIDE	10 mg/1	30 TABLET in 1 BOTTLE (13107-104-30)
13107-104-99	13107-104	HUMAN PRESCRIPTION DRUG	Oxymorphone Hydrochloride	Oxymorphone Hydrochloride	TABLET	ORAL	20160426	N/A	ANDA	ANDA204459	Aurolife Pharma, LLC	OXYMORPHONE HYDROCHLORIDE	10 mg/1	1000 TABLET in 1 BOTTLE (13107-104-99)
13107-103-01	13107-103	HUMAN PRESCRIPTION DRUG	Oxymorphone Hydrochloride	Oxymorphone Hydrochloride	TABLET	ORAL	20160426	N/A	ANDA	ANDA204459	Aurolife Pharma, LLC	OXYMORPHONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (13107-103-01)
13107-103-30	13107-103	HUMAN PRESCRIPTION DRUG	Oxymorphone Hydrochloride	Oxymorphone Hydrochloride	TABLET	ORAL	20160426	N/A	ANDA	ANDA204459	Aurolife Pharma, LLC	OXYMORPHONE HYDROCHLORIDE	5 mg/1	30 TABLET in 1 BOTTLE (13107-103-30)
13107-103-99	13107-103	HUMAN PRESCRIPTION DRUG	Oxymorphone Hydrochloride	Oxymorphone Hydrochloride	TABLET	ORAL	20160426	N/A	ANDA	ANDA204459	Aurolife Pharma, LLC	OXYMORPHONE HYDROCHLORIDE	5 mg/1	1000 TABLET in 1 BOTTLE (13107-103-99)