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
69367-449-01	69367-449	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260309	N/A	ANDA	ANDA215318	Westminster Pharmaceuticals, LLC	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69367-449-01)
69367-449-05	69367-449	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260309	N/A	ANDA	ANDA215318	Westminster Pharmaceuticals, LLC	IBUPROFEN	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69367-449-05)
69367-447-01	69367-447	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260309	N/A	ANDA	ANDA215318	Westminster Pharmaceuticals, LLC	IBUPROFEN	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69367-447-01)
69367-447-05	69367-447	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260309	N/A	ANDA	ANDA215318	Westminster Pharmaceuticals, LLC	IBUPROFEN	400 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69367-447-05)
69367-448-01	69367-448	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260309	N/A	ANDA	ANDA215318	Westminster Pharmaceuticals, LLC	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69367-448-01)
69367-448-05	69367-448	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20260309	N/A	ANDA	ANDA215318	Westminster Pharmaceuticals, LLC	IBUPROFEN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69367-448-05)