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
72603-158-02	72603-158	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20230705	N/A	ANDA	ANDA202862	NorthStar RxLLC	OLANZAPINE	15 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72603-158-02)
0615-8566-39	0615-8566	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20250225	N/A	ANDA	ANDA202862	NCS HealthCare of KY, LLC dba Vangard Labs	OLANZAPINE	15 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8566-39)
72603-154-02	72603-154	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20230705	N/A	ANDA	ANDA202862	NorthStar RxLLC	OLANZAPINE	2.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72603-154-02)
72603-154-03	72603-154	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20230705	N/A	ANDA	ANDA202862	NorthStar RxLLC	OLANZAPINE	2.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72603-154-03)
72603-155-01	72603-155	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20230705	N/A	ANDA	ANDA202862	NorthStar RxLLC	OLANZAPINE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72603-155-01)
70518-0921-0	70518-0921	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20171226	N/A	ANDA	ANDA202862	REMEDYREPACK INC.	OLANZAPINE	10 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0921-0)
70518-0935-0	70518-0935	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20180105	N/A	ANDA	ANDA202862	REMEDYREPACK INC.	OLANZAPINE	5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0935-0)
71335-0534-3	71335-0534	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20210601	N/A	ANDA	ANDA202862	Bryant Ranch Prepack	OLANZAPINE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0534-3)
71335-0534-5	71335-0534	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA202862	Bryant Ranch Prepack	OLANZAPINE	5 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0534-5)
71335-0534-4	71335-0534	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA202862	Bryant Ranch Prepack	OLANZAPINE	5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0534-4)
71335-0534-1	71335-0534	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20180221	N/A	ANDA	ANDA202862	Bryant Ranch Prepack	OLANZAPINE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0534-1)
71335-0534-2	71335-0534	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA202862	Bryant Ranch Prepack	OLANZAPINE	5 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-0534-2)
71335-9661-1	71335-9661	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20230306	N/A	ANDA	ANDA202862	Bryant Ranch Prepack	OLANZAPINE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-9661-1)
71335-9661-2	71335-9661	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20230306	N/A	ANDA	ANDA202862	Bryant Ranch Prepack	OLANZAPINE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-9661-2)
72603-159-01	72603-159	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20230705	N/A	ANDA	ANDA202862	NorthStar RxLLC	OLANZAPINE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72603-159-01)
72603-159-02	72603-159	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20230705	N/A	ANDA	ANDA202862	NorthStar RxLLC	OLANZAPINE	20 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72603-159-02)
71335-9661-3	71335-9661	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20230306	N/A	ANDA	ANDA202862	Bryant Ranch Prepack	OLANZAPINE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-9661-3)
72162-2368-0	72162-2368	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20240716	N/A	ANDA	ANDA202862	Bryant Ranch Prepack	OLANZAPINE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72162-2368-0)
72189-578-30	72189-578	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20240917	N/A	ANDA	ANDA202862	Direct_Rx	OLANZAPINE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-578-30)
72603-159-03	72603-159	HUMAN PRESCRIPTION DRUG	Olanzapine	Olanzapine	TABLET, FILM COATED	ORAL	20230705	N/A	ANDA	ANDA202862	NorthStar RxLLC	OLANZAPINE	20 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (72603-159-03)