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
71610-523-30	71610-523	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20210203	N/A	ANDA	ANDA076122	Aphena Pharma Solutions - Tennessee, LLC	MIRTAZAPINE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-523-30)
71610-523-45	71610-523	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20210423	N/A	ANDA	ANDA076122	Aphena Pharma Solutions - Tennessee, LLC	MIRTAZAPINE	30 mg/1	45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-523-45)
71610-523-53	71610-523	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20210804	N/A	ANDA	ANDA076122	Aphena Pharma Solutions - Tennessee, LLC	MIRTAZAPINE	30 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-523-53)
71610-523-60	71610-523	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20210212	N/A	ANDA	ANDA076122	Aphena Pharma Solutions - Tennessee, LLC	MIRTAZAPINE	30 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-523-60)
51407-350-30	51407-350	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20200221	N/A	ANDA	ANDA076122	Golden State Medical Supply, Inc.	MIRTAZAPINE	15 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-350-30)
51407-351-05	51407-351	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20200221	N/A	ANDA	ANDA076122	Golden State Medical Supply, Inc.	MIRTAZAPINE	30 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-351-05)
51407-351-30	51407-351	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20200221	N/A	ANDA	ANDA076122	Golden State Medical Supply, Inc.	MIRTAZAPINE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-351-30)