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
65862-032-90	65862-032	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20041022	N/A	ANDA	ANDA076921	Aurobindo Pharma Limited	MIRTAZAPINE	45 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-032-90)
68788-7251-1	68788-7251	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20180828	N/A	ANDA	ANDA076921	Preferred Pharmaceuticals Inc.	MIRTAZAPINE	15 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (68788-7251-1)
68788-7251-3	68788-7251	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20180828	N/A	ANDA	ANDA076921	Preferred Pharmaceuticals Inc.	MIRTAZAPINE	15 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7251-3)
68788-7251-6	68788-7251	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20180828	N/A	ANDA	ANDA076921	Preferred Pharmaceuticals Inc.	MIRTAZAPINE	15 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7251-6)
68788-7251-9	68788-7251	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20180828	N/A	ANDA	ANDA076921	Preferred Pharmaceuticals Inc.	MIRTAZAPINE	15 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7251-9)
71205-481-30	71205-481	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20201001	N/A	ANDA	ANDA076921	Proficient Rx LP	MIRTAZAPINE	15 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-481-30)
71205-481-60	71205-481	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20201001	N/A	ANDA	ANDA076921	Proficient Rx LP	MIRTAZAPINE	15 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-481-60)
71205-481-90	71205-481	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20201001	N/A	ANDA	ANDA076921	Proficient Rx LP	MIRTAZAPINE	15 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-481-90)