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
70408-239-32	70408-239	HUMAN PRESCRIPTION DRUG	NITROFURANTOIN	NITROFURANTOIN	SUSPENSION	ORAL	20120304	N/A	ANDA	ANDA201355	Nostrum Laboratories, Inc.	NITROFURANTOIN	25 mg/5mL	240 mL in 1 BOTTLE, PLASTIC (70408-239-32)
29033-515-32	29033-515	HUMAN PRESCRIPTION DRUG	NITROFURANTOIN	Nitrofurantoin	SUSPENSION	ORAL	20240216	N/A	ANDA	ANDA201355	Nostrum Laboratories, Inc.	NITROFURANTOIN	25 mg/5mL	240 mL in 1 BOTTLE, PLASTIC (29033-515-32)
29033-515-34	29033-515	HUMAN PRESCRIPTION DRUG	NITROFURANTOIN	Nitrofurantoin	SUSPENSION	ORAL	20240216	N/A	ANDA	ANDA201355	Nostrum Laboratories, Inc.	NITROFURANTOIN	25 mg/5mL	480 mL in 1 BOTTLE, PLASTIC (29033-515-34)
0121-1996-95	0121-1996	HUMAN PRESCRIPTION DRUG	Nitrofurantoin Oral Suspension	Nitrofurantoin Oral Suspension	SUSPENSION	ORAL	20240610	N/A	ANDA	ANDA201355	PAI Holdings, LLC dba PAI Pharma	NITROFURANTOIN	25 mg/5mL	10 CUP, UNIT-DOSE in 1 CASE (0121-1996-95) / 10 mL in 1 CUP, UNIT-DOSE (0121-1996-10)