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
71921-180-01	71921-180	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211021	N/A	ANDA	ANDA071268	Florida Pharmaceutical Products, LLC	IBUPROFEN	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71921-180-01)
71921-180-50	71921-180	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211021	N/A	ANDA	ANDA071268	Florida Pharmaceutical Products, LLC	IBUPROFEN	400 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71921-180-50)
71921-181-01	71921-181	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211021	N/A	ANDA	ANDA071268	Florida Pharmaceutical Products, LLC	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71921-181-01)
71921-181-50	71921-181	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211021	N/A	ANDA	ANDA071268	Florida Pharmaceutical Products, LLC	IBUPROFEN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71921-181-50)
71921-182-01	71921-182	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211021	N/A	ANDA	ANDA071268	Florida Pharmaceutical Products, LLC	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71921-182-01)
71921-182-50	71921-182	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20211021	N/A	ANDA	ANDA071268	Florida Pharmaceutical Products, LLC	IBUPROFEN	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (71921-182-50)
68071-2939-4	68071-2939	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20230216	N/A	ANDA	ANDA071268	NuCare Pharmaceuticals,Inc.	IBUPROFEN	400 mg/1	4 TABLET, FILM COATED in 1 BOTTLE (68071-2939-4)
68071-2939-6	68071-2939	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20230216	N/A	ANDA	ANDA071268	NuCare Pharmaceuticals,Inc.	IBUPROFEN	400 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-2939-6)