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
68084-875-01	68084-875	HUMAN PRESCRIPTION DRUG	Montelukast Sodium	Montelukast Sodium	TABLET, COATED	ORAL	20150402	N/A	ANDA	ANDA201582	American Health Packaging	MONTELUKAST SODIUM	10 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-875-01) / 1 TABLET, COATED in 1 BLISTER PACK (68084-875-11)
70518-1784-1	70518-1784	HUMAN PRESCRIPTION DRUG	Montelukast Sodium	Montelukast Sodium	TABLET, COATED	ORAL	20231211	N/A	ANDA	ANDA201582	REMEDYREPACK INC.	MONTELUKAST SODIUM	10 mg/1	30 TABLET, COATED in 1 BLISTER PACK (70518-1784-1)
55111-725-01	55111-725	HUMAN PRESCRIPTION DRUG	Montelukast Sodium	Montelukast Sodium	TABLET, COATED	ORAL	20120806	N/A	ANDA	ANDA201582	Dr.Reddy's Laboratories Limited	MONTELUKAST SODIUM	10 mg/1	100 TABLET, COATED in 1 BOTTLE (55111-725-01)
55111-725-10	55111-725	HUMAN PRESCRIPTION DRUG	Montelukast Sodium	Montelukast Sodium	TABLET, COATED	ORAL	20120806	N/A	ANDA	ANDA201582	Dr.Reddy's Laboratories Limited	MONTELUKAST SODIUM	10 mg/1	1000 TABLET, COATED in 1 BOTTLE (55111-725-10)
55111-725-30	55111-725	HUMAN PRESCRIPTION DRUG	Montelukast Sodium	Montelukast Sodium	TABLET, COATED	ORAL	20120806	N/A	ANDA	ANDA201582	Dr.Reddy's Laboratories Limited	MONTELUKAST SODIUM	10 mg/1	30 TABLET, COATED in 1 BOTTLE (55111-725-30)
55111-725-78	55111-725	HUMAN PRESCRIPTION DRUG	Montelukast Sodium	Montelukast Sodium	TABLET, COATED	ORAL	20120806	N/A	ANDA	ANDA201582	Dr.Reddy's Laboratories Limited	MONTELUKAST SODIUM	10 mg/1	10 BLISTER PACK in 1 CARTON (55111-725-78) / 10 TABLET, COATED in 1 BLISTER PACK (55111-725-79)
55111-725-90	55111-725	HUMAN PRESCRIPTION DRUG	Montelukast Sodium	Montelukast Sodium	TABLET, COATED	ORAL	20120806	N/A	ANDA	ANDA201582	Dr.Reddy's Laboratories Limited	MONTELUKAST SODIUM	10 mg/1	90 TABLET, COATED in 1 BOTTLE (55111-725-90)