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
71930-045-52	71930-045	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; 5 mg/1	500 TABLET in 1 BOTTLE (71930-045-52)
0904-7093-61	0904-7093	HUMAN PRESCRIPTION DRUG	OXYCODONE AND ACETAMINOPHEN	oxycodone and acetaminophen	TABLET	ORAL	20190601	N/A	ANDA	ANDA207510	Major Pharmaceuticals	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 5 mg/1	100 BLISTER PACK in 1 CARTON (0904-7093-61) / 1 TABLET in 1 BLISTER PACK
71335-9674-8	71335-9674	HUMAN PRESCRIPTION DRUG	OXYCODONE AND ACETAMINOPHEN	oxycodone and acetaminophen	TABLET	ORAL	20230327	N/A	ANDA	ANDA207510	Bryant Ranch Prepack	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 5 mg/1	60 TABLET in 1 BOTTLE (71335-9674-8)
71335-9674-9	71335-9674	HUMAN PRESCRIPTION DRUG	OXYCODONE AND ACETAMINOPHEN	oxycodone and acetaminophen	TABLET	ORAL	20230327	N/A	ANDA	ANDA207510	Bryant Ranch Prepack	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 5 mg/1	84 TABLET in 1 BOTTLE (71335-9674-9)