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
65162-464-10	65162-464	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals LLC	IBUPROFEN	400 mg/1	100 TABLET in 1 BOTTLE (65162-464-10)
82982-033-60	82982-033	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20230308	20251231	ANDA	ANDA078558	Pharmasource Meds, LLC	IBUPROFEN	800 mg/1	60 TABLET in 1 BOTTLE (82982-033-60)
80425-0047-4	80425-0047	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	30 TABLET in 1 BOTTLE (80425-0047-4)
80425-0047-5	80425-0047	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	100 TABLET in 1 BOTTLE (80425-0047-5)
80425-0047-1	80425-0047	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (80425-0047-1)
80425-0047-2	80425-0047	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	120 TABLET in 1 BOTTLE (80425-0047-2)
80425-0047-3	80425-0047	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	60 TABLET in 1 BOTTLE (80425-0047-3)
53746-464-01	53746-464	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	400 mg/1	100 TABLET in 1 BOTTLE (53746-464-01)
53746-464-90	53746-464	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	400 mg/1	90 TABLET in 1 BOTTLE (53746-464-90)
53746-465-01	53746-465	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	600 mg/1	100 TABLET in 1 BOTTLE (53746-465-01)
53746-465-05	53746-465	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	600 mg/1	500 TABLET in 1 BOTTLE (53746-465-05)
53746-465-30	53746-465	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	600 mg/1	30 TABLET in 1 BOTTLE (53746-465-30)
53746-465-50	53746-465	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	600 mg/1	50 TABLET in 1 BOTTLE (53746-465-50)
53746-465-60	53746-465	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	600 mg/1	60 TABLET in 1 BOTTLE (53746-465-60)
53746-465-90	53746-465	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	600 mg/1	90 TABLET in 1 BOTTLE (53746-465-90)
53746-466-01	53746-466	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	100 TABLET in 1 BOTTLE (53746-466-01)
53746-466-05	53746-466	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	500 TABLET in 1 BOTTLE (53746-466-05)
53746-466-30	53746-466	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	30 TABLET in 1 BOTTLE (53746-466-30)
53746-466-50	53746-466	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	50 TABLET in 1 BOTTLE (53746-466-50)
53746-466-60	53746-466	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20091123	N/A	ANDA	ANDA078558	Amneal Pharmaceuticals of New York LLC	IBUPROFEN	800 mg/1	60 TABLET in 1 BOTTLE (53746-466-60)