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
0527-1671-01	0527-1671	HUMAN PRESCRIPTION DRUG	Oxycodone and Acetaminophen	Oxycodone and Acetaminophen	TABLET	ORAL	20170925	N/A	ANDA	ANDA207333	Lannett Company, Inc.	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 10 mg/1	100 TABLET in 1 BOTTLE (0527-1671-01)
0527-1669-05	0527-1669	HUMAN PRESCRIPTION DRUG	Oxycodone and Acetaminophen	Oxycodone and Acetaminophen	TABLET	ORAL	20170925	N/A	ANDA	ANDA207333	Lannett Company, Inc.	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 5 mg/1	500 TABLET in 1 BOTTLE (0527-1669-05)
0527-1669-01	0527-1669	HUMAN PRESCRIPTION DRUG	Oxycodone and Acetaminophen	Oxycodone and Acetaminophen	TABLET	ORAL	20170925	N/A	ANDA	ANDA207333	Lannett Company, Inc.	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 5 mg/1	100 TABLET in 1 BOTTLE (0527-1669-01)
0527-1671-05	0527-1671	HUMAN PRESCRIPTION DRUG	Oxycodone and Acetaminophen	Oxycodone and Acetaminophen	TABLET	ORAL	20170925	N/A	ANDA	ANDA207333	Lannett Company, Inc.	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 10 mg/1	500 TABLET in 1 BOTTLE (0527-1671-05)