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
0591-2998-01	0591-2998	HUMAN PRESCRIPTION DRUG	Ursodiol	Ursodiol	TABLET	ORAL	19971210	N/A	NDA AUTHORIZED GENERIC	NDA020675	Actavis Pharma, Inc.	URSODIOL	250 mg/1	100 TABLET in 1 BOTTLE (0591-2998-01)
0591-3005-01	0591-3005	HUMAN PRESCRIPTION DRUG	Ursodiol	Ursodiol	TABLET	ORAL	19971210	N/A	NDA AUTHORIZED GENERIC	NDA020675	Actavis Pharma, Inc.	URSODIOL	500 mg/1	100 TABLET in 1 BOTTLE (0591-3005-01)
58914-785-10	58914-785	HUMAN PRESCRIPTION DRUG	Urso 250	Ursodiol	TABLET, FILM COATED	ORAL	19971210	N/A	NDA	NDA020675	Allergan, Inc.	URSODIOL	250 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (58914-785-10)
58914-790-01	58914-790	HUMAN PRESCRIPTION DRUG	Urso Forte	Ursodiol	TABLET, FILM COATED	ORAL	19971210	N/A	NDA	NDA020675	Allergan, Inc.	URSODIOL	500 mg/1	4 TABLET, FILM COATED in 1 BLISTER PACK (58914-790-01)
58914-790-10	58914-790	HUMAN PRESCRIPTION DRUG	Urso Forte	Ursodiol	TABLET, FILM COATED	ORAL	19971210	N/A	NDA	NDA020675	Allergan, Inc.	URSODIOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (58914-790-10)