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
67296-1655-7	67296-1655	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA204575	RedPharm Drug, Inc.	HYDROCODONE BITARTRATE; IBUPROFEN	7.5 mg/1; 200 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (67296-1655-7)
13107-004-01	13107-004	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET, FILM COATED	ORAL	20160602	N/A	ANDA	ANDA204575	Aurolife Pharma, LLC	HYDROCODONE BITARTRATE; IBUPROFEN	7.5 mg/1; 200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (13107-004-01)
13107-004-05	13107-004	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET, FILM COATED	ORAL	20160602	N/A	ANDA	ANDA204575	Aurolife Pharma, LLC	HYDROCODONE BITARTRATE; IBUPROFEN	7.5 mg/1; 200 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (13107-004-05)
13107-004-11	13107-004	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET, FILM COATED	ORAL	20160602	N/A	ANDA	ANDA204575	Aurolife Pharma, LLC	HYDROCODONE BITARTRATE; IBUPROFEN	7.5 mg/1; 200 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (13107-004-11)
13107-004-99	13107-004	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET, FILM COATED	ORAL	20160602	N/A	ANDA	ANDA204575	Aurolife Pharma, LLC	HYDROCODONE BITARTRATE; IBUPROFEN	7.5 mg/1; 200 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (13107-004-99)