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
0781-5827-01	0781-5827	HUMAN PRESCRIPTION DRUG	Ultramicrosize Griseofulvin	Ultramicrosize Griseofulvin	TABLET, COATED	ORAL	20200401	N/A	ANDA	ANDA202805	Sandoz Inc	GRISEOFULVIN	125 mg/1	100 TABLET, COATED in 1 BOTTLE (0781-5827-01)
0781-5827-05	0781-5827	HUMAN PRESCRIPTION DRUG	Ultramicrosize Griseofulvin	Ultramicrosize Griseofulvin	TABLET, COATED	ORAL	20200401	N/A	ANDA	ANDA202805	Sandoz Inc	GRISEOFULVIN	125 mg/1	500 TABLET, COATED in 1 BOTTLE (0781-5827-05)
0781-5828-01	0781-5828	HUMAN PRESCRIPTION DRUG	Ultramicrosize Griseofulvin	Ultramicrosize Griseofulvin	TABLET, COATED	ORAL	20200401	N/A	ANDA	ANDA202805	Sandoz Inc	GRISEOFULVIN	250 mg/1	100 TABLET, COATED in 1 BOTTLE (0781-5828-01)
0781-5828-05	0781-5828	HUMAN PRESCRIPTION DRUG	Ultramicrosize Griseofulvin	Ultramicrosize Griseofulvin	TABLET, COATED	ORAL	20200401	N/A	ANDA	ANDA202805	Sandoz Inc	GRISEOFULVIN	250 mg/1	500 TABLET, COATED in 1 BOTTLE (0781-5828-05)