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
68071-2536-6	68071-2536	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20210916	N/A	ANDA	ANDA202116	NuCare Pharmaceuticals,Inc,	OXYCODONE HYDROCHLORIDE	5 mg/1	6 TABLET in 1 BOTTLE (68071-2536-6)
47781-263-01	47781-263	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20111230	N/A	ANDA	ANDA202116	Alvogen, Inc.	OXYCODONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (47781-263-01)
47781-263-05	47781-263	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20111230	N/A	ANDA	ANDA202116	Alvogen, Inc.	OXYCODONE HYDROCHLORIDE	5 mg/1	500 TABLET in 1 BOTTLE (47781-263-05)
47781-264-01	47781-264	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20111230	N/A	ANDA	ANDA202116	Alvogen, Inc.	OXYCODONE HYDROCHLORIDE	15 mg/1	100 TABLET in 1 BOTTLE (47781-264-01)
47781-264-05	47781-264	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20111230	N/A	ANDA	ANDA202116	Alvogen, Inc.	OXYCODONE HYDROCHLORIDE	15 mg/1	500 TABLET in 1 BOTTLE (47781-264-05)
47781-265-01	47781-265	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20111230	N/A	ANDA	ANDA202116	Alvogen, Inc.	OXYCODONE HYDROCHLORIDE	30 mg/1	100 TABLET in 1 BOTTLE (47781-265-01)
47781-265-05	47781-265	HUMAN PRESCRIPTION DRUG	Oxycodone hydrochloride	Oxycodone hydrochloride	TABLET	ORAL	20111230	N/A	ANDA	ANDA202116	Alvogen, Inc.	OXYCODONE HYDROCHLORIDE	30 mg/1	500 TABLET in 1 BOTTLE (47781-265-05)