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
66993-606-04	66993-606	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20230601	N/A	ANDA	ANDA216751	Prasco Laboratories	MIRTAZAPINE	7.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (66993-606-04)
66993-606-30	66993-606	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20230601	N/A	ANDA	ANDA216751	Prasco Laboratories	MIRTAZAPINE	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (66993-606-30)
66993-607-04	66993-607	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20230901	N/A	ANDA	ANDA216751	Prasco Laboratories	MIRTAZAPINE	15 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (66993-607-04)
66993-607-30	66993-607	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20230901	N/A	ANDA	ANDA216751	Prasco Laboratories	MIRTAZAPINE	15 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (66993-607-30)
66993-608-04	66993-608	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20230901	N/A	ANDA	ANDA216751	Prasco Laboratories	MIRTAZAPINE	30 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (66993-608-04)
66993-608-30	66993-608	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20230901	N/A	ANDA	ANDA216751	Prasco Laboratories	MIRTAZAPINE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (66993-608-30)
66993-609-04	66993-609	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20230901	N/A	ANDA	ANDA216751	Prasco Laboratories	MIRTAZAPINE	45 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (66993-609-04)
66993-609-30	66993-609	HUMAN PRESCRIPTION DRUG	Mirtazapine	Mirtazapine	TABLET, FILM COATED	ORAL	20230901	N/A	ANDA	ANDA216751	Prasco Laboratories	MIRTAZAPINE	45 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (66993-609-30)