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
68180-401-01	68180-401	HUMAN PRESCRIPTION DRUG	CEFPROZIL	CEFPROZIL	POWDER, FOR SUSPENSION	ORAL	20051201	N/A	ANDA	ANDA065261	Lupin Pharmaceuticals, Inc.	CEFPROZIL	125 mg/5mL	50 mL in 1 BOTTLE (68180-401-01)
68180-401-02	68180-401	HUMAN PRESCRIPTION DRUG	CEFPROZIL	CEFPROZIL	POWDER, FOR SUSPENSION	ORAL	20051201	N/A	ANDA	ANDA065261	Lupin Pharmaceuticals, Inc.	CEFPROZIL	125 mg/5mL	75 mL in 1 BOTTLE (68180-401-02)
68180-401-03	68180-401	HUMAN PRESCRIPTION DRUG	CEFPROZIL	CEFPROZIL	POWDER, FOR SUSPENSION	ORAL	20051201	N/A	ANDA	ANDA065261	Lupin Pharmaceuticals, Inc.	CEFPROZIL	125 mg/5mL	100 mL in 1 BOTTLE (68180-401-03)
68180-402-01	68180-402	HUMAN PRESCRIPTION DRUG	CEFPROZIL	CEFPROZIL	POWDER, FOR SUSPENSION	ORAL	20051201	N/A	ANDA	ANDA065261	Lupin Pharmaceuticals, Inc.	CEFPROZIL	250 mg/5mL	50 mL in 1 BOTTLE (68180-402-01)
68180-402-02	68180-402	HUMAN PRESCRIPTION DRUG	CEFPROZIL	CEFPROZIL	POWDER, FOR SUSPENSION	ORAL	20051201	N/A	ANDA	ANDA065261	Lupin Pharmaceuticals, Inc.	CEFPROZIL	250 mg/5mL	75 mL in 1 BOTTLE (68180-402-02)
68180-402-03	68180-402	HUMAN PRESCRIPTION DRUG	CEFPROZIL	CEFPROZIL	POWDER, FOR SUSPENSION	ORAL	20051201	N/A	ANDA	ANDA065261	Lupin Pharmaceuticals, Inc.	CEFPROZIL	250 mg/5mL	100 mL in 1 BOTTLE (68180-402-03)