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
53746-117-01	53746-117	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET	ORAL	20100218	N/A	ANDA	ANDA076642	Amneal Pharmaceuticals of New York LLC	HYDROCODONE BITARTRATE; IBUPROFEN	10 mg/1; 200 mg/1	100 TABLET in 1 BOTTLE (53746-117-01)
53746-146-01	53746-146	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET	ORAL	20100218	N/A	ANDA	ANDA076642	Amneal Pharmaceuticals of New York LLC	HYDROCODONE BITARTRATE; IBUPROFEN	5 mg/1; 200 mg/1	100 TABLET in 1 BOTTLE (53746-146-01)
53746-116-01	53746-116	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET	ORAL	20100218	N/A	ANDA	ANDA076642	Amneal Pharmaceuticals of New York LLC	HYDROCODONE BITARTRATE; IBUPROFEN	2.5 mg/1; 200 mg/1	100 TABLET in 1 BOTTLE (53746-116-01)
53746-145-05	53746-145	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET	ORAL	20100218	N/A	ANDA	ANDA076642	Amneal Pharmaceuticals of New York LLC	HYDROCODONE BITARTRATE; IBUPROFEN	7.5 mg/1; 200 mg/1	500 TABLET in 1 BOTTLE (53746-145-05)
53746-145-01	53746-145	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET	ORAL	20100218	N/A	ANDA	ANDA076642	Amneal Pharmaceuticals of New York LLC	HYDROCODONE BITARTRATE; IBUPROFEN	7.5 mg/1; 200 mg/1	100 TABLET in 1 BOTTLE (53746-145-01)
68084-841-01	68084-841	HUMAN PRESCRIPTION DRUG	Hydrocodone Bitartrate and Ibuprofen	Hydrocodone Bitartrate and Ibuprofen	TABLET	ORAL	20150213	20240930	ANDA	ANDA076642	American Health Packaging	HYDROCODONE BITARTRATE; IBUPROFEN	7.5 mg/1; 200 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-841-01) / 1 TABLET in 1 BLISTER PACK (68084-841-11)