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
70518-3313-0	70518-3313	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211228	N/A	ANDA	ANDA090796	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3313-0)
80425-0089-1	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0089-1)
80425-0089-2	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0089-2)
80425-0089-3	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (80425-0089-3)
80425-0089-4	80425-0089	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0089-4)
80425-0132-1	80425-0132	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx Pharmacy of Tennessee, LLC	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0132-1)
80425-0132-2	80425-0132	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx Pharmacy of Tennessee, LLC	IBUPROFEN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0132-2)
80425-0132-3	80425-0132	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	Advanced Rx Pharmacy of Tennessee, LLC	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0132-3)
80425-0243-4	80425-0243	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20230110	N/A	ANDA	ANDA090796	Advanced Rx Pharmacy of Tennessee, LLC	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (80425-0243-4)
80425-0393-1	80425-0393	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240523	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	30 TABLET in 1 BOTTLE (80425-0393-1)
80425-0393-2	80425-0393	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240523	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	60 TABLET in 1 BOTTLE (80425-0393-2)
80425-0393-3	80425-0393	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240523	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	90 TABLET in 1 BOTTLE (80425-0393-3)
80425-0393-4	80425-0393	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240523	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	100 TABLET in 1 BOTTLE (80425-0393-4)
80425-0393-5	80425-0393	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240523	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	800 mg/1	120 TABLET in 1 BOTTLE (80425-0393-5)
80425-0426-1	80425-0426	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240806	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	600 mg/1	30 TABLET in 1 BOTTLE (80425-0426-1)
80425-0426-2	80425-0426	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240806	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	600 mg/1	60 TABLET in 1 BOTTLE (80425-0426-2)
80425-0426-3	80425-0426	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240806	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	600 mg/1	90 TABLET in 1 BOTTLE (80425-0426-3)
80425-0426-4	80425-0426	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET	ORAL	20240806	N/A	ANDA	ANDA090796	Advanced Rx of Tennessee, LLC	IBUPROFEN	600 mg/1	100 TABLET in 1 BOTTLE (80425-0426-4)
68071-3362-0	68071-3362	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170726	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	12 TABLET, FILM COATED in 1 BOTTLE (68071-3362-0)
68071-3362-1	68071-3362	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170726	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (68071-3362-1)