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
71335-2182-6	71335-2182	HUMAN PRESCRIPTION DRUG	ENDOCET	Oxycodone and Acetaminophen	TABLET	ORAL	20240812	N/A	ANDA	ANDA040330	Bryant Ranch Prepack	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 10 mg/1	20 TABLET in 1 BOTTLE (71335-2182-6)
71335-2182-7	71335-2182	HUMAN PRESCRIPTION DRUG	ENDOCET	Oxycodone and Acetaminophen	TABLET	ORAL	20240812	N/A	ANDA	ANDA040330	Bryant Ranch Prepack	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 10 mg/1	45 TABLET in 1 BOTTLE (71335-2182-7)
71335-2182-8	71335-2182	HUMAN PRESCRIPTION DRUG	ENDOCET	Oxycodone and Acetaminophen	TABLET	ORAL	20240812	N/A	ANDA	ANDA040330	Bryant Ranch Prepack	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 10 mg/1	75 TABLET in 1 BOTTLE (71335-2182-8)
71335-2182-9	71335-2182	HUMAN PRESCRIPTION DRUG	ENDOCET	Oxycodone and Acetaminophen	TABLET	ORAL	20240812	N/A	ANDA	ANDA040330	Bryant Ranch Prepack	ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE	325 mg/1; 10 mg/1	100 TABLET in 1 BOTTLE (71335-2182-9)