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
68084-740-01	68084-740	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20140522	N/A	ANDA	ANDA076255	American Health Packaging	OLANZAPINE	10 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-740-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-740-11)
70518-1635-0	70518-1635	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20181106	N/A	ANDA	ANDA076255	REMEDYREPACK INC.	OLANZAPINE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1635-0)
70518-1611-2	70518-1611	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20250207	N/A	ANDA	ANDA076255	REMEDYREPACK INC.	OLANZAPINE	7.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1611-2)
70518-1605-0	70518-1605	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20181026	N/A	ANDA	ANDA076255	REMEDYREPACK INC.	OLANZAPINE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1605-0)
70518-1611-0	70518-1611	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20181029	N/A	ANDA	ANDA076255	REMEDYREPACK INC.	OLANZAPINE	7.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1611-0)
70518-1764-0	70518-1764	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20190102	N/A	ANDA	ANDA076255	REMEDYREPACK INC.	OLANZAPINE	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1764-0)