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
60505-3140-8	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)
63187-844-90	63187-844	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20170501	N/A	ANDA	ANDA090798	Proficient Rx LP	OLANZAPINE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-844-90)
53002-1505-3	53002-1505	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20181001	N/A	ANDA	ANDA090798	RPK Pharmaceuticals, Inc.	OLANZAPINE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-1505-3)
60505-3113-0	60505-3113	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20120423	N/A	ANDA	ANDA090798	Apotex Corp.	OLANZAPINE	10 mg/1	10 BLISTER PACK in 1 CARTON (60505-3113-0) / 10 TABLET, FILM COATED in 1 BLISTER PACK
60505-3113-8	60505-3113	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20120423	N/A	ANDA	ANDA090798	Apotex Corp.	OLANZAPINE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (60505-3113-8)