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
71335-0714-1	71335-0714	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20180302	N/A	ANDA	ANDA076255	Bryant Ranch Prepack	OLANZAPINE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0714-1)
71335-0714-2	71335-0714	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA076255	Bryant Ranch Prepack	OLANZAPINE	5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-0714-2)
71335-0714-3	71335-0714	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA076255	Bryant Ranch Prepack	OLANZAPINE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0714-3)
71335-0714-4	71335-0714	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA076255	Bryant Ranch Prepack	OLANZAPINE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0714-4)
71335-0714-5	71335-0714	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA076255	Bryant Ranch Prepack	OLANZAPINE	5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0714-5)
70518-0110-0	70518-0110	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20170110	N/A	ANDA	ANDA076255	REMEDYREPACK INC.	OLANZAPINE	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0110-0)