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
0378-3530-05	0378-3530	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20030620	N/A	ANDA	ANDA076122	Mylan Pharmaceuticals Inc.	MIRTAZAPINE	30 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3530-05)
0378-3530-93	0378-3530	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20030620	N/A	ANDA	ANDA076122	Mylan Pharmaceuticals Inc.	MIRTAZAPINE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3530-93)
0378-3545-01	0378-3545	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20160802	N/A	ANDA	ANDA076122	Mylan Pharmaceuticals Inc.	MIRTAZAPINE	45 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3545-01)
0378-3515-93	0378-3515	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20030620	N/A	ANDA	ANDA076122	Mylan Pharmaceuticals Inc.	MIRTAZAPINE	15 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3515-93)
0378-3515-10	0378-3515	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20030620	N/A	ANDA	ANDA076122	Mylan Pharmaceuticals Inc.	MIRTAZAPINE	15 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3515-10)
0378-3515-01	0378-3515	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20160802	N/A	ANDA	ANDA076122	Mylan Pharmaceuticals Inc.	MIRTAZAPINE	15 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3515-01)
0378-3545-05	0378-3545	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20030620	N/A	ANDA	ANDA076122	Mylan Pharmaceuticals Inc.	MIRTAZAPINE	45 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3545-05)
0378-3545-93	0378-3545	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20030620	N/A	ANDA	ANDA076122	Mylan Pharmaceuticals Inc.	MIRTAZAPINE	45 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3545-93)