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
63304-497-01	63304-497	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20180731	N/A	ANDA	ANDA040826	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	100 TABLET in 1 BOTTLE (63304-497-01)
63304-497-03	63304-497	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20180731	N/A	ANDA	ANDA040826	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	10 TABLET in 1 BOTTLE (63304-497-03)
63304-497-05	63304-497	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20180731	N/A	ANDA	ANDA040826	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	500 TABLET in 1 BOTTLE (63304-497-05)
63304-497-10	63304-497	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20180731	N/A	ANDA	ANDA040826	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	1000 TABLET in 1 BOTTLE (63304-497-10)
63304-497-69	63304-497	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Acetaminophen	Hydrocodone Bitartrate and Acetaminophen	TABLET	ORAL	20180731	N/A	ANDA	ANDA040826	Sun Pharmaceutical Industries, Inc.	ACETAMINOPHEN; HYDROCODONE BITARTRATE	325 mg/1; 10 mg/1	10 BLISTER PACK in 1 CARTON (63304-497-69) / 1 TABLET in 1 BLISTER PACK (63304-497-11)