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
68462-473-05	68462-473	HUMAN PRESCRIPTION DRUG	Ursodiol	Ursodiol	TABLET	ORAL	20110712	N/A	ANDA	ANDA090801	Glenmark Pharmaceuticals Inc., USA	URSODIOL	250 mg/1	500 TABLET in 1 BOTTLE (68462-473-05)
68462-473-30	68462-473	HUMAN PRESCRIPTION DRUG	Ursodiol	Ursodiol	TABLET	ORAL	20110712	N/A	ANDA	ANDA090801	Glenmark Pharmaceuticals Inc., USA	URSODIOL	250 mg/1	30 TABLET in 1 BOTTLE (68462-473-30)
68462-474-01	68462-474	HUMAN PRESCRIPTION DRUG	Ursodiol	Ursodiol	TABLET	ORAL	20110712	N/A	ANDA	ANDA090801	Glenmark Pharmaceuticals Inc., USA	URSODIOL	500 mg/1	100 TABLET in 1 BOTTLE (68462-474-01)
68462-474-05	68462-474	HUMAN PRESCRIPTION DRUG	Ursodiol	Ursodiol	TABLET	ORAL	20110712	N/A	ANDA	ANDA090801	Glenmark Pharmaceuticals Inc., USA	URSODIOL	500 mg/1	500 TABLET in 1 BOTTLE (68462-474-05)
68462-474-30	68462-474	HUMAN PRESCRIPTION DRUG	Ursodiol	Ursodiol	TABLET	ORAL	20110712	N/A	ANDA	ANDA090801	Glenmark Pharmaceuticals Inc., USA	URSODIOL	500 mg/1	30 TABLET in 1 BOTTLE (68462-474-30)
68462-473-01	68462-473	HUMAN PRESCRIPTION DRUG	Ursodiol	Ursodiol	TABLET	ORAL	20110712	N/A	ANDA	ANDA090801	Glenmark Pharmaceuticals Inc., USA	URSODIOL	250 mg/1	100 TABLET in 1 BOTTLE (68462-473-01)
68001-378-00	68001-378	HUMAN PRESCRIPTION DRUG	Ursodiol	Ursodiol	TABLET	ORAL	20190226	N/A	ANDA	ANDA090801	BluePoint Laboratories	URSODIOL	500 mg/1	100 TABLET in 1 BOTTLE (68001-378-00)
68001-377-00	68001-377	HUMAN PRESCRIPTION DRUG	Ursodiol	Ursodiol	TABLET	ORAL	20190226	N/A	ANDA	ANDA090801	BluePoint Laboratories	URSODIOL	250 mg/1	100 TABLET in 1 BOTTLE (68001-377-00)