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
72578-062-16	72578-062	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20190416	N/A	ANDA	ANDA206747	Viona Pharmaceuticals Inc	VORICONAZOLE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72578-062-16)
72578-062-77	72578-062	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20190416	N/A	ANDA	ANDA206747	Viona Pharmaceuticals Inc	VORICONAZOLE	50 mg/1	10 BLISTER PACK in 1 CARTON (72578-062-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (72578-062-30)
72578-063-16	72578-063	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20190416	N/A	ANDA	ANDA206747	Viona Pharmaceuticals Inc	VORICONAZOLE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72578-063-16)
72578-063-10	72578-063	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20190416	N/A	ANDA	ANDA206747	Viona Pharmaceuticals Inc	VORICONAZOLE	200 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72578-063-10)
72578-063-06	72578-063	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20190416	N/A	ANDA	ANDA206747	Viona Pharmaceuticals Inc	VORICONAZOLE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72578-063-06)