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
67296-1040-2	67296-1040	HUMAN PRESCRIPTION DRUG	oxycodone hydrochloride	oxycodone hydrochloride	TABLET	ORAL	20090512	N/A	ANDA	ANDA090659	RedPharm Drug, Inc.	OXYCODONE HYDROCHLORIDE	5 mg/1	20 TABLET in 1 BOTTLE (67296-1040-2)
67296-1040-4	67296-1040	HUMAN PRESCRIPTION DRUG	oxycodone hydrochloride	oxycodone hydrochloride	TABLET	ORAL	20090512	N/A	ANDA	ANDA090659	RedPharm Drug, Inc.	OXYCODONE HYDROCHLORIDE	5 mg/1	40 TABLET in 1 BOTTLE (67296-1040-4)
57664-187-88	57664-187	HUMAN PRESCRIPTION DRUG	oxycodone hydrochloride	oxycodone hydrochloride	TABLET	ORAL	20090512	N/A	ANDA	ANDA090659	Sun Pharmaceutical Industries, Inc.	OXYCODONE HYDROCHLORIDE	15 mg/1	100 TABLET in 1 BOTTLE (57664-187-88)
57664-223-88	57664-223	HUMAN PRESCRIPTION DRUG	oxycodone hydrochloride	oxycodone hydrochloride	TABLET	ORAL	20090512	N/A	ANDA	ANDA090659	Sun Pharmaceutical Industries, Inc.	OXYCODONE HYDROCHLORIDE	5 mg/1	100 TABLET in 1 BOTTLE (57664-223-88)
57664-224-88	57664-224	HUMAN PRESCRIPTION DRUG	oxycodone hydrochloride	oxycodone hydrochloride	TABLET	ORAL	20090512	N/A	ANDA	ANDA090659	Sun Pharmaceutical Industries, Inc.	OXYCODONE HYDROCHLORIDE	30 mg/1	100 TABLET in 1 BOTTLE (57664-224-88)
57664-370-88	57664-370	HUMAN PRESCRIPTION DRUG	oxycodone hydrochloride	oxycodone hydrochloride	TABLET	ORAL	20121119	N/A	ANDA	ANDA090659	Sun Pharmaceutical Industries, Inc.	OXYCODONE HYDROCHLORIDE	10 mg/1	100 TABLET in 1 BOTTLE (57664-370-88)
57664-371-88	57664-371	HUMAN PRESCRIPTION DRUG	oxycodone hydrochloride	oxycodone hydrochloride	TABLET	ORAL	20121119	N/A	ANDA	ANDA090659	Sun Pharmaceutical Industries, Inc.	OXYCODONE HYDROCHLORIDE	20 mg/1	100 TABLET in 1 BOTTLE (57664-371-88)