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
60687-294-21	60687-294	HUMAN PRESCRIPTION DRUG	Voriconazole	Voriconazole	TABLET, FILM COATED	ORAL	20180307	N/A	ANDA	ANDA203503	American Health Packaging	VORICONAZOLE	50 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-294-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-294-11)
60687-273-21	60687-273	HUMAN PRESCRIPTION DRUG	Voriconazole	Voriconazole	TABLET, FILM COATED	ORAL	20170811	N/A	ANDA	ANDA203503	American Health Packaging	VORICONAZOLE	200 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-273-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-273-11)
68462-573-13	68462-573	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20150904	N/A	ANDA	ANDA203503	Glenmark Pharmaceuticals Inc., USA	VORICONAZOLE	200 mg/1	3 BLISTER PACK in 1 CARTON (68462-573-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68462-573-30	68462-573	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20150904	N/A	ANDA	ANDA203503	Glenmark Pharmaceuticals Inc., USA	VORICONAZOLE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-573-30)
68462-573-90	68462-573	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20150904	N/A	ANDA	ANDA203503	Glenmark Pharmaceuticals Inc., USA	VORICONAZOLE	200 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68462-573-90)
51407-133-30	51407-133	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20180905	N/A	ANDA	ANDA203503	Golden State Medical Supply, Inc.	VORICONAZOLE	200 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (51407-133-30)
68462-572-13	68462-572	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20150904	N/A	ANDA	ANDA203503	Glenmark Pharmaceuticals Inc., USA	VORICONAZOLE	50 mg/1	3 BLISTER PACK in 1 CARTON (68462-572-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68462-572-30	68462-572	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20150904	N/A	ANDA	ANDA203503	Glenmark Pharmaceuticals Inc., USA	VORICONAZOLE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68462-572-30)
68462-572-90	68462-572	HUMAN PRESCRIPTION DRUG	voriconazole	voriconazole	TABLET, FILM COATED	ORAL	20150904	N/A	ANDA	ANDA203503	Glenmark Pharmaceuticals Inc., USA	VORICONAZOLE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68462-572-90)