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
71335-1979-3	71335-1979	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20211221	N/A	ANDA	ANDA202843	Bryant Ranch Prepack	MONTELUKAST SODIUM	10 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-1979-3)
71335-1979-4	71335-1979	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20211221	N/A	ANDA	ANDA202843	Bryant Ranch Prepack	MONTELUKAST SODIUM	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1979-4)
71335-1979-5	71335-1979	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20211221	N/A	ANDA	ANDA202843	Bryant Ranch Prepack	MONTELUKAST SODIUM	10 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-1979-5)
71335-1979-6	71335-1979	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20211027	N/A	ANDA	ANDA202843	Bryant Ranch Prepack	MONTELUKAST SODIUM	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1979-6)
71335-1979-7	71335-1979	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20211221	N/A	ANDA	ANDA202843	Bryant Ranch Prepack	MONTELUKAST SODIUM	10 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1979-7)
71335-1979-8	71335-1979	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20211221	N/A	ANDA	ANDA202843	Bryant Ranch Prepack	MONTELUKAST SODIUM	10 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1979-8)
68788-8099-3	68788-8099	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20211006	N/A	ANDA	ANDA202843	Preferred Pharmaceuticals, Inc.	MONTELUKAST SODIUM	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8099-3)
68788-8099-6	68788-8099	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20211006	N/A	ANDA	ANDA202843	Preferred Pharmaceuticals, Inc.	MONTELUKAST SODIUM	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8099-6)
68788-8099-9	68788-8099	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20211006	N/A	ANDA	ANDA202843	Preferred Pharmaceuticals, Inc.	MONTELUKAST SODIUM	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8099-9)
82009-009-10	82009-009	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20220607	N/A	ANDA	ANDA202843	Quallent Pharmaceuticals Health LLC	MONTELUKAST SODIUM	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (82009-009-10)
50268-556-15	50268-556	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20220208	N/A	ANDA	ANDA202843	AvPAK	MONTELUKAST SODIUM	10 mg/1	50 BLISTER PACK in 1 BOX (50268-556-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-556-11)
0904-6808-06	0904-6808	HUMAN PRESCRIPTION DRUG	Montelukast Sodium	Montelukast Sodium	TABLET, FILM COATED	ORAL	20140910	N/A	ANDA	ANDA202843	Major Pharmaceuticals	MONTELUKAST SODIUM	10 mg/1	50 BLISTER PACK in 1 CARTON (0904-6808-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-6808-61	0904-6808	HUMAN PRESCRIPTION DRUG	Montelukast Sodium	Montelukast Sodium	TABLET, FILM COATED	ORAL	20140910	N/A	ANDA	ANDA202843	Major Pharmaceuticals	MONTELUKAST SODIUM	10 mg/1	100 BLISTER PACK in 1 CARTON (0904-6808-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK