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
72162-1475-0	72162-1475	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET	ORAL	20240206	20240831	ANDA	ANDA088262	Bryant Ranch Prepack	IMIPRAMINE HYDROCHLORIDE	25 mg/1	1000 TABLET in 1 BOTTLE (72162-1475-0)
70518-1793-1	70518-1793	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET	ORAL	20201218	20240831	ANDA	ANDA088262	REMEDYREPACK INC.	IMIPRAMINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BLISTER PACK (70518-1793-1)
49884-055-01	49884-055	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET	ORAL	19831101	20240831	ANDA	ANDA088262	Par Pharmaceutical, Inc.	IMIPRAMINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (49884-055-01)
49884-055-10	49884-055	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET	ORAL	19831101	20240831	ANDA	ANDA088262	Par Pharmaceutical, Inc.	IMIPRAMINE HYDROCHLORIDE	25 mg/1	1000 TABLET in 1 BOTTLE (49884-055-10)
64380-170-01	64380-170	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET	ORAL	20220509	N/A	ANDA	ANDA088262	Strides Pharma Science Limited	IMIPRAMINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (64380-170-01)
64380-170-02	64380-170	HUMAN PRESCRIPTION DRUG	Imipramine Hydrochloride	Imipramine Hydrochloride	TABLET	ORAL	20220509	N/A	ANDA	ANDA088262	Strides Pharma Science Limited	IMIPRAMINE HYDROCHLORIDE	25 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (64380-170-02)