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
80425-0294-3	80425-0294	HUMAN PRESCRIPTION DRUG	Imipramine hydrochloride	Imipramine hydrochloride	TABLET, FILM COATED	ORAL	20230404	N/A	ANDA	ANDA040903	Advanced Rx Pharmacy of Tennessee, LLC	IMIPRAMINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0294-3)
80425-0294-2	80425-0294	HUMAN PRESCRIPTION DRUG	Imipramine hydrochloride	Imipramine hydrochloride	TABLET, FILM COATED	ORAL	20230404	N/A	ANDA	ANDA040903	Advanced Rx Pharmacy of Tennessee, LLC	IMIPRAMINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0294-2)
80425-0294-1	80425-0294	HUMAN PRESCRIPTION DRUG	Imipramine hydrochloride	Imipramine hydrochloride	TABLET, FILM COATED	ORAL	20230404	N/A	ANDA	ANDA040903	Advanced Rx Pharmacy of Tennessee, LLC	IMIPRAMINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0294-1)
71205-804-30	71205-804	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20230605	N/A	ANDA	ANDA040903	Proficient Rx LP	IMIPRAMINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-804-30)
71205-804-60	71205-804	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20230605	N/A	ANDA	ANDA040903	Proficient Rx LP	IMIPRAMINE HYDROCHLORIDE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-804-60)
71205-804-90	71205-804	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20230605	N/A	ANDA	ANDA040903	Proficient Rx LP	IMIPRAMINE HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-804-90)
50090-3148-0	50090-3148	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20171003	N/A	ANDA	ANDA040903	A-S Medication Solutions	IMIPRAMINE HYDROCHLORIDE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-3148-0)
70518-1588-0	70518-1588	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20181025	N/A	ANDA	ANDA040903	REMEDYREPACK INC.	IMIPRAMINE HYDROCHLORIDE	50 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1588-0)
69315-134-01	69315-134	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20160412	N/A	ANDA	ANDA040903	Leading Pharma, LLC	IMIPRAMINE HYDROCHLORIDE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69315-134-01)
69315-135-01	69315-135	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20160412	N/A	ANDA	ANDA040903	Leading Pharma, LLC	IMIPRAMINE HYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69315-135-01)
69315-135-10	69315-135	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20160501	N/A	ANDA	ANDA040903	Leading Pharma, LLC	IMIPRAMINE HYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69315-135-10)
69315-133-01	69315-133	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20160407	N/A	ANDA	ANDA040903	Leading Pharma, LLC	IMIPRAMINE HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69315-133-01)
69315-133-10	69315-133	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20160414	N/A	ANDA	ANDA040903	Leading Pharma, LLC	IMIPRAMINE HYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69315-133-10)
69315-134-10	69315-134	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20160501	N/A	ANDA	ANDA040903	Leading Pharma, LLC	IMIPRAMINE HYDROCHLORIDE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (69315-134-10)
55700-709-30	55700-709	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET, FILM COATED	ORAL	20181214	N/A	ANDA	ANDA040903	Quality Care Products, LLC	IMIPRAMINE HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (55700-709-30)