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
72865-131-01	72865-131	HUMAN PRESCRIPTION DRUG	OXYMORPHONE HYDROCHLORIDE	OXYMORPHONE HYDROCHLORIDE	TABLET	ORAL	20200506	N/A	ANDA	ANDA210175	XLCare Pharmaceuticals, Inc.	OXYMORPHONE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (72865-131-01)
63629-1926-1	63629-1926	HUMAN PRESCRIPTION DRUG	OXYMORPHONE HYDROCHLORIDE	OXYMORPHONE HYDROCHLORIDE	TABLET	ORAL	20210114	N/A	ANDA	ANDA210175	Bryant Ranch Prepack	OXYMORPHONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (63629-1926-1)
72865-130-01	72865-130	HUMAN PRESCRIPTION DRUG	OXYMORPHONE HYDROCHLORIDE	OXYMORPHONE HYDROCHLORIDE	TABLET	ORAL	20200506	N/A	ANDA	ANDA210175	XLCare Pharmaceuticals, Inc.	OXYMORPHONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (72865-130-01)
31722-930-01	31722-930	HUMAN PRESCRIPTION DRUG	OXYMORPHONE HYDROCHLORIDE	OXYMORPHONE HYDROCHLORIDE	TABLET	ORAL	20180301	N/A	ANDA	ANDA210175	Camber Pharmaceuticals, Inc	OXYMORPHONE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (31722-930-01)
31722-929-01	31722-929	HUMAN PRESCRIPTION DRUG	OXYMORPHONE HYDROCHLORIDE	OXYMORPHONE HYDROCHLORIDE	TABLET	ORAL	20180301	N/A	ANDA	ANDA210175	Camber Pharmaceuticals, Inc	OXYMORPHONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (31722-929-01)