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
64850-631-01	64850-631	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20181116	N/A	ANDA	ANDA209924	Elite Laboratories, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 5 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (64850-631-01)
64850-630-01	64850-630	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20181116	N/A	ANDA	ANDA209924	Elite Laboratories, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 2.5 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (64850-630-01)
64850-633-01	64850-633	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20181116	N/A	ANDA	ANDA209924	Elite Laboratories, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (64850-633-01)
64850-632-01	64850-632	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20181116	N/A	ANDA	ANDA209924	Elite Laboratories, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 7.5 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (64850-632-01)