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
72189-266-60	72189-266	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210916	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	800 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-266-60)
72189-266-71	72189-266	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210916	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72189-266-71)
72189-266-72	72189-266	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210916	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	800 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (72189-266-72)
72189-266-90	72189-266	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210916	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-266-90)
72189-266-15	72189-266	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210916	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (72189-266-15)
72189-324-30	72189-324	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20220221	N/A	ANDA	ANDA090796	Direct Rx	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-324-30)
72189-324-60	72189-324	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20220221	N/A	ANDA	ANDA090796	Direct Rx	IBUPROFEN	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-324-60)