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
60505-3111-0	60505-3111	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20120423	N/A	ANDA	ANDA090798	Apotex Corp.	OLANZAPINE	5 mg/1	10 BLISTER PACK in 1 CARTON (60505-3111-0) / 10 TABLET, FILM COATED in 1 BLISTER PACK
60505-3111-8	60505-3111	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20120423	N/A	ANDA	ANDA090798	Apotex Corp.	OLANZAPINE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-3111-8)
60505-3140-0	60505-3140	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20120423	N/A	ANDA	ANDA090798	Apotex Corp.	OLANZAPINE	20 mg/1	10 BLISTER PACK in 1 CARTON (60505-3140-0) / 10 TABLET, FILM COATED in 1 BLISTER PACK
60505-3140-3	60505-3140	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20120423	N/A	ANDA	ANDA090798	Apotex Corp.	OLANZAPINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (60505-3140-3)
60505-3140-8	60505-3140	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20120423	N/A	ANDA	ANDA090798	Apotex Corp.	OLANZAPINE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-3140-8)