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
71930-046-52	71930-046	HUMAN PRESCRIPTION DRUG	OXYCODONE AND ACETAMINOPHEN	oxycodone and acetaminophen	TABLET	ORAL	20190601	N/A	ANDA	ANDA207510	Eywa Pharma Inc	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 7.5 mg/1	500 TABLET in 1 BOTTLE (71930-046-52)
71930-047-12	71930-047	HUMAN PRESCRIPTION DRUG	OXYCODONE AND ACETAMINOPHEN	oxycodone and acetaminophen	TABLET	ORAL	20190601	N/A	ANDA	ANDA207510	Eywa Pharma Inc	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 10 mg/1	100 TABLET in 1 BOTTLE (71930-047-12)
71930-047-52	71930-047	HUMAN PRESCRIPTION DRUG	OXYCODONE AND ACETAMINOPHEN	oxycodone and acetaminophen	TABLET	ORAL	20190601	N/A	ANDA	ANDA207510	Eywa Pharma Inc	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 10 mg/1	500 TABLET in 1 BOTTLE (71930-047-52)