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
70518-0314-1	70518-0314	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20220610	N/A	ANDA	ANDA090798	REMEDYREPACK INC.	OLANZAPINE	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0314-1)
63187-844-03	63187-844	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20170501	N/A	ANDA	ANDA090798	Proficient Rx LP	OLANZAPINE	5 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (63187-844-03)
63187-844-30	63187-844	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20120423	N/A	ANDA	ANDA090798	Proficient Rx LP	OLANZAPINE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-844-30)
63187-844-60	63187-844	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20120423	N/A	ANDA	ANDA090798	Proficient Rx LP	OLANZAPINE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-844-60)
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)