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
72865-175-30	72865-175	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20210211	N/A	ANDA	ANDA202843	XLCare Pharmaceuticals Inc.	MONTELUKAST SODIUM	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72865-175-30)
72865-175-90	72865-175	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20210211	N/A	ANDA	ANDA202843	XLCare Pharmaceuticals Inc.	MONTELUKAST SODIUM	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72865-175-90)
50090-6108-0	50090-6108	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20220928	N/A	ANDA	ANDA202843	A-S Medication Solutions	MONTELUKAST SODIUM	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-6108-0)
50090-6108-1	50090-6108	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20220928	N/A	ANDA	ANDA202843	A-S Medication Solutions	MONTELUKAST SODIUM	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6108-1)
55154-8075-0	55154-8075	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20140910	N/A	ANDA	ANDA202843	Cardinal Health 107, LLC	MONTELUKAST SODIUM	10 mg/1	10 BLISTER PACK in 1 BAG (55154-8075-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
70518-3133-0	70518-3133	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20210618	N/A	ANDA	ANDA202843	REMEDYREPACK INC.	MONTELUKAST SODIUM	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3133-0)
70518-3133-1	70518-3133	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20210701	N/A	ANDA	ANDA202843	REMEDYREPACK INC.	MONTELUKAST SODIUM	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3133-1)
68071-1561-3	68071-1561	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20210913	N/A	ANDA	ANDA202843	NuCare Pharmaceuticals,Inc.	MONTELUKAST SODIUM	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-1561-3)
53002-6441-1	53002-6441	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20230101	N/A	ANDA	ANDA202843	RPK Pharmaceuticals, Inc.	MONTELUKAST SODIUM	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-6441-1)
53002-6441-2	53002-6441	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20230101	N/A	ANDA	ANDA202843	RPK Pharmaceuticals, Inc.	MONTELUKAST SODIUM	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (53002-6441-2)
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)
50090-6109-0	50090-6109	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20220928	N/A	ANDA	ANDA202843	A-S Medication Solutions	MONTELUKAST SODIUM	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-6109-0)
71610-563-30	71610-563	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20210527	N/A	ANDA	ANDA202843	Aphena Pharma Solutions - Tennessee, LLC	MONTELUKAST SODIUM	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71610-563-30)
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)
31722-726-32	31722-726	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20140910	N/A	ANDA	ANDA202843	Camber Pharmaceuticals, Inc.	MONTELUKAST SODIUM	10 mg/1	10 TABLET, FILM COATED in 1 CARTON (31722-726-32)
31722-726-90	31722-726	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20140910	N/A	ANDA	ANDA202843	Camber Pharmaceuticals, Inc.	MONTELUKAST SODIUM	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-726-90)
68645-560-54	68645-560	HUMAN PRESCRIPTION DRUG	Montelukast	Montelukast	TABLET, FILM COATED	ORAL	20140910	N/A	ANDA	ANDA202843	Legacy Pharmaceutical Packaging, LLC	MONTELUKAST SODIUM	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68645-560-54)