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
70518-4322-0	70518-4322	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20250328	N/A	ANDA	ANDA076122	REMEDYREPACK INC.	MIRTAZAPINE	15 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4322-0)
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)
51407-352-05	51407-352	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20200221	N/A	ANDA	ANDA076122	Golden State Medical Supply, Inc.	MIRTAZAPINE	45 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-352-05)
51407-352-30	51407-352	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20200221	N/A	ANDA	ANDA076122	Golden State Medical Supply, Inc.	MIRTAZAPINE	45 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-352-30)
51407-350-10	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	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-350-10)
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)
55154-5355-0	55154-5355	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20091130	N/A	ANDA	ANDA076122	Cardinal Health 107, LLC	MIRTAZAPINE	15 mg/1	10 BLISTER PACK in 1 BAG (55154-5355-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK