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
42291-970-60	42291-970	HUMAN PRESCRIPTION DRUG	Zafirlukast	zafirlukast	TABLET, COATED	ORAL	20230405	N/A	NDA	NDA020547	AvKARE	ZAFIRLUKAST	10 mg/1	60 TABLET, COATED in 1 BOTTLE (42291-970-60)
64380-187-01	64380-187	HUMAN PRESCRIPTION DRUG	Zafirlukast	zafirlukast	TABLET, COATED	ORAL	20220915	N/A	NDA	NDA020547	Strides Pharma Science Limited	ZAFIRLUKAST	10 mg/1	60 TABLET, COATED in 1 BOTTLE (64380-187-01)
42291-971-60	42291-971	HUMAN PRESCRIPTION DRUG	Zafirlukast	zafirlukast	TABLET, COATED	ORAL	20230405	N/A	NDA	NDA020547	AvKARE	ZAFIRLUKAST	20 mg/1	60 TABLET, COATED in 1 BOTTLE (42291-971-60)
49884-554-02	49884-554	HUMAN PRESCRIPTION DRUG	Zafirlukast	zafirlukast	TABLET, COATED	ORAL	20101119	20240930	NDA	NDA020547	Par Pharmaceutical, Inc.	ZAFIRLUKAST	20 mg/1	60 TABLET, COATED in 1 BOTTLE (49884-554-02)
64380-178-01	64380-178	HUMAN PRESCRIPTION DRUG	ACCOLATE	Zafirlukast	TABLET, FILM COATED	ORAL	20230102	N/A	NDA	NDA020547	Strides Pharma Science Limited	ZAFIRLUKAST	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (64380-178-01)
72162-2362-6	72162-2362	HUMAN PRESCRIPTION DRUG	Zafirlukast	zafirlukast	TABLET, COATED	ORAL	20240628	N/A	NDA	NDA020547	Bryant Ranch Prepack	ZAFIRLUKAST	20 mg/1	60 TABLET, COATED in 1 BOTTLE (72162-2362-6)
64380-177-01	64380-177	HUMAN PRESCRIPTION DRUG	ACCOLATE	Zafirlukast	TABLET, FILM COATED	ORAL	20230102	N/A	NDA	NDA020547	Strides Pharma Science Limited	ZAFIRLUKAST	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (64380-177-01)
64380-188-01	64380-188	HUMAN PRESCRIPTION DRUG	Zafirlukast	zafirlukast	TABLET, COATED	ORAL	20220801	N/A	NDA	NDA020547	Strides Pharma Science Limited	ZAFIRLUKAST	20 mg/1	60 TABLET, COATED in 1 BOTTLE (64380-188-01)