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
71335-1218-8	71335-1218	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (71335-1218-8)
71335-1218-9	71335-1218	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1218-9)
71335-1073-7	71335-1073	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20190219	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1073-7)
71335-1218-0	71335-1218	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-1218-0)
71335-1218-1	71335-1218	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20220209	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1218-1)