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
33342-102-07	33342-102	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET	ORAL	20140911	N/A	ANDA	ANDA203366	Macleods Pharmaceuticals Limited	MONTELUKAST SODIUM	10 mg/1	30 TABLET in 1 BOTTLE (33342-102-07)
33342-102-10	33342-102	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET	ORAL	20140911	N/A	ANDA	ANDA203366	Macleods Pharmaceuticals Limited	MONTELUKAST SODIUM	10 mg/1	90 TABLET in 1 BOTTLE (33342-102-10)
33342-102-12	33342-102	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET	ORAL	20140911	N/A	ANDA	ANDA203366	Macleods Pharmaceuticals Limited	MONTELUKAST SODIUM	10 mg/1	100 TABLET in 1 BLISTER PACK (33342-102-12)
33342-102-15	33342-102	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET	ORAL	20140911	N/A	ANDA	ANDA203366	Macleods Pharmaceuticals Limited	MONTELUKAST SODIUM	10 mg/1	500 TABLET in 1 BOTTLE (33342-102-15)
33342-102-39	33342-102	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET	ORAL	20140911	N/A	ANDA	ANDA203366	Macleods Pharmaceuticals Limited	MONTELUKAST SODIUM	10 mg/1	90 TABLET in 1 BLISTER PACK (33342-102-39)
68001-361-05	68001-361	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET	ORAL	20180629	N/A	ANDA	ANDA203366	BluePoint Laboratories	MONTELUKAST SODIUM	10 mg/1	90 TABLET in 1 BOTTLE (68001-361-05)
68001-361-03	68001-361	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET	ORAL	20180629	N/A	ANDA	ANDA203366	BluePoint Laboratories	MONTELUKAST SODIUM	10 mg/1	500 TABLET in 1 BOTTLE (68001-361-03)
68001-361-04	68001-361	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET	ORAL	20180629	N/A	ANDA	ANDA203366	BluePoint Laboratories	MONTELUKAST SODIUM	10 mg/1	30 TABLET in 1 BOTTLE (68001-361-04)
68071-4034-9	68071-4034	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET	ORAL	20170808	N/A	ANDA	ANDA203366	NuCare Pharmaceuticals,Inc.	MONTELUKAST SODIUM	10 mg/1	90 TABLET in 1 BOTTLE (68071-4034-9)