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
51079-164-03	51079-164	HUMAN PRESCRIPTION DRUG	Voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20110808	20241231	ANDA	ANDA090547	Mylan Institutional Inc.	VORICONAZOLE	50 mg/1	30 BLISTER PACK in 1 CARTON (51079-164-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-164-01)
51079-165-03	51079-165	HUMAN PRESCRIPTION DRUG	Voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20110808	20241231	ANDA	ANDA090547	Mylan Institutional Inc.	VORICONAZOLE	200 mg/1	30 BLISTER PACK in 1 CARTON (51079-165-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-165-01)
0378-1626-93	0378-1626	HUMAN PRESCRIPTION DRUG	Voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20110215	20241231	ANDA	ANDA090547	Mylan Pharmaceuticals Inc.	VORICONAZOLE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1626-93)
0378-1640-93	0378-1640	HUMAN PRESCRIPTION DRUG	Voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20110215	20241231	ANDA	ANDA090547	Mylan Pharmaceuticals Inc.	VORICONAZOLE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1640-93)