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
87063-049-05	87063-049	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20251124	N/A	ANDA	ANDA210211	Asclemed USA, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 5 mg/1	5 TABLET in 1 BOTTLE (87063-049-05)
87063-049-07	87063-049	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20251124	N/A	ANDA	ANDA210211	Asclemed USA, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 5 mg/1	7 TABLET in 1 BOTTLE (87063-049-07)
87063-049-10	87063-049	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20251124	N/A	ANDA	ANDA210211	Asclemed USA, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 5 mg/1	10 TABLET in 1 BOTTLE (87063-049-10)