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
0115-1316-08	0115-1316	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	15 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1316-08)
0115-1316-13	0115-1316	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	15 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1316-13)
0115-1315-03	0115-1315	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	7.5 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-03)
0115-1315-08	0115-1315	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-08)
64896-701-01	64896-701	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-701-01)
64896-701-03	64896-701	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	40 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-701-03)
64896-701-08	64896-701	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-701-08)
64896-701-13	64896-701	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	40 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-701-13)
0115-1315-13	0115-1315	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1315-13)
0115-1233-03	0115-1233	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	20 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-03)
0115-1233-08	0115-1233	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-08)
0115-1233-13	0115-1233	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	20 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1233-13)
0115-1317-01	0115-1317	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	30 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1317-01)
0115-1317-03	0115-1317	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	30 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1317-03)
0115-1317-08	0115-1317	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	30 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1317-08)
0115-1317-13	0115-1317	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals of New York LLC	OXYMORPHONE HYDROCHLORIDE	30 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1317-13)