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
64850-623-01	64850-623	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride and Acetaminophen	Oxycodone Hydrochloride and Acetaminophen	TABLET	ORAL	20171204	N/A	ANDA	ANDA209385	Elite Laboratories, Inc.	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 10 mg/1	100 TABLET in 1 BOTTLE (64850-623-01)
64850-622-01	64850-622	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride and Acetaminophen	Oxycodone Hydrochloride and Acetaminophen	TABLET	ORAL	20171204	N/A	ANDA	ANDA209385	Elite Laboratories, Inc.	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 7.5 mg/1	100 TABLET in 1 BOTTLE (64850-622-01)
64850-621-01	64850-621	HUMAN PRESCRIPTION DRUG	Oxycodone Hydrochloride and Acetaminophen	Oxycodone Hydrochloride and Acetaminophen	TABLET	ORAL	20240711	N/A	ANDA	ANDA209385	Elite Laboratories, Inc.	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 5 mg/1	100 TABLET in 1 BOTTLE (64850-621-01)