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
64896-696-01	64896-696	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	7.5 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-01)
64896-696-03	64896-696	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	7.5 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-03)
64896-696-08	64896-696	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	7.5 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-08)
64896-696-13	64896-696	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-696-13)
64896-700-01	64896-700	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	30 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-700-01)
64896-700-03	64896-700	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	30 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-700-03)
64896-700-08	64896-700	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	30 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-700-08)
64896-700-13	64896-700	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	30 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-700-13)
0115-1231-01	0115-1231	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	5 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1231-01)
64896-697-01	64896-697	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-01)
64896-697-03	64896-697	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-03)
64896-697-08	64896-697	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-08)
64896-697-13	64896-697	HUMAN PRESCRIPTION DRUG	Oxymorphone hydrochloride	Oxymorphone hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20130102	N/A	ANDA	ANDA079087	Amneal Pharmaceuticals LLC	OXYMORPHONE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (64896-697-13)
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)
0115-1232-01	0115-1232	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	10 mg/1	100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1232-01)
0115-1232-03	0115-1232	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	10 mg/1	1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1232-03)
0115-1232-08	0115-1232	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	10 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-1232-08)