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
27241-018-03	27241-018	HUMAN PRESCRIPTION DRUG	MONTELUKAST SODIUM	MONTELUKAST SODIUM	TABLET, COATED	ORAL	20150813	N/A	ANDA	ANDA203432	Ajanta Pharma USA Inc.	MONTELUKAST SODIUM	10 mg/1	30 TABLET, COATED in 1 BOTTLE (27241-018-03)
27241-018-09	27241-018	HUMAN PRESCRIPTION DRUG	MONTELUKAST SODIUM	MONTELUKAST SODIUM	TABLET, COATED	ORAL	20150813	N/A	ANDA	ANDA203432	Ajanta Pharma USA Inc.	MONTELUKAST SODIUM	10 mg/1	90 TABLET, COATED in 1 BOTTLE (27241-018-09)
27241-018-90	27241-018	HUMAN PRESCRIPTION DRUG	MONTELUKAST SODIUM	MONTELUKAST SODIUM	TABLET, COATED	ORAL	20150813	N/A	ANDA	ANDA203432	Ajanta Pharma USA Inc.	MONTELUKAST SODIUM	10 mg/1	1000 TABLET, COATED in 1 BOTTLE (27241-018-90)
63187-692-30	63187-692	HUMAN PRESCRIPTION DRUG	MONTELUKAST SODIUM	MONTELUKAST SODIUM	TABLET, COATED	ORAL	20160401	N/A	ANDA	ANDA203432	Proficient Rx LP	MONTELUKAST SODIUM	10 mg/1	30 TABLET, COATED in 1 BOTTLE (63187-692-30)
63187-692-60	63187-692	HUMAN PRESCRIPTION DRUG	MONTELUKAST SODIUM	MONTELUKAST SODIUM	TABLET, COATED	ORAL	20160401	N/A	ANDA	ANDA203432	Proficient Rx LP	MONTELUKAST SODIUM	10 mg/1	60 TABLET, COATED in 1 BOTTLE (63187-692-60)
63187-692-90	63187-692	HUMAN PRESCRIPTION DRUG	MONTELUKAST SODIUM	MONTELUKAST SODIUM	TABLET, COATED	ORAL	20160401	N/A	ANDA	ANDA203432	Proficient Rx LP	MONTELUKAST SODIUM	10 mg/1	90 TABLET, COATED in 1 BOTTLE (63187-692-90)