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
72162-1816-9	72162-1816	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET	ORAL	20230508	N/A	ANDA	ANDA076820	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET in 1 BOTTLE (72162-1816-9)
51655-755-26	51655-755	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET	ORAL	20231114	N/A	ANDA	ANDA076820	Northwind Pharmaceuticals, LLC	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-755-26)
51655-755-52	51655-755	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET	ORAL	20230403	N/A	ANDA	ANDA076820	Northwind Pharmaceuticals, LLC	BENAZEPRIL HYDROCHLORIDE	20 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-755-52)
70518-3528-0	70518-3528	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET	ORAL	20220920	N/A	ANDA	ANDA076820	REMEDYREPACK INC.	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-3528-0)