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
31722-007-01	31722-007	HUMAN PRESCRIPTION DRUG	Zafirlukast	Zafirlukast	TABLET, FILM COATED	ORAL	20200910	N/A	ANDA	ANDA212475	Camber Pharmaceuticals, Inc.	ZAFIRLUKAST	10 mg/1	10 BLISTER PACK in 1 CARTON (31722-007-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK
31722-007-05	31722-007	HUMAN PRESCRIPTION DRUG	Zafirlukast	Zafirlukast	TABLET, FILM COATED	ORAL	20200910	N/A	ANDA	ANDA212475	Camber Pharmaceuticals, Inc.	ZAFIRLUKAST	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-007-05)
31722-007-60	31722-007	HUMAN PRESCRIPTION DRUG	Zafirlukast	Zafirlukast	TABLET, FILM COATED	ORAL	20200910	N/A	ANDA	ANDA212475	Camber Pharmaceuticals, Inc.	ZAFIRLUKAST	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (31722-007-60)
31722-008-01	31722-008	HUMAN PRESCRIPTION DRUG	Zafirlukast	Zafirlukast	TABLET, FILM COATED	ORAL	20200910	N/A	ANDA	ANDA212475	Camber Pharmaceuticals, Inc.	ZAFIRLUKAST	20 mg/1	10 BLISTER PACK in 1 CARTON (31722-008-01) / 10 TABLET, FILM COATED in 1 BLISTER PACK
31722-008-05	31722-008	HUMAN PRESCRIPTION DRUG	Zafirlukast	Zafirlukast	TABLET, FILM COATED	ORAL	20200910	N/A	ANDA	ANDA212475	Camber Pharmaceuticals, Inc.	ZAFIRLUKAST	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (31722-008-05)
31722-008-60	31722-008	HUMAN PRESCRIPTION DRUG	Zafirlukast	Zafirlukast	TABLET, FILM COATED	ORAL	20200910	N/A	ANDA	ANDA212475	Camber Pharmaceuticals, Inc.	ZAFIRLUKAST	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (31722-008-60)
72162-2361-6	72162-2361	HUMAN PRESCRIPTION DRUG	Zafirlukast	Zafirlukast	TABLET, FILM COATED	ORAL	20240628	N/A	ANDA	ANDA212475	Bryant Ranch Prepack	ZAFIRLUKAST	20 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72162-2361-6)