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
51655-202-26	51655-202	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20230315	N/A	ANDA	ANDA078212	Northwind Pharmaceuticals, LLC	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-202-26)
71335-1365-3	71335-1365	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20240530	N/A	ANDA	ANDA078212	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1365-3)
68071-2929-9	68071-2929	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20230206	N/A	ANDA	ANDA078212	NuCare Pharmaceuticals,Inc.	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-2929-9)
51655-617-26	51655-617	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20220906	N/A	ANDA	ANDA078212	Northwind Pharmaceuticals, LLC	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (51655-617-26)
51655-617-52	51655-617	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20230920	N/A	ANDA	ANDA078212	Northwind Pharmaceuticals, LLC	BENAZEPRIL HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-617-52)
70518-3074-1	70518-3074	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20220509	N/A	ANDA	ANDA078212	REMEDYREPACK INC.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3074-1)
70518-3171-1	70518-3171	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20221206	N/A	ANDA	ANDA078212	REMEDYREPACK INC.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3171-1)
50090-5750-0	50090-5750	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20210930	N/A	ANDA	ANDA078212	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-5750-0)
50090-5750-1	50090-5750	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20210930	N/A	ANDA	ANDA078212	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5750-1)
71335-1365-2	71335-1365	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20191007	N/A	ANDA	ANDA078212	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1365-2)
71335-1365-1	71335-1365	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20200213	N/A	ANDA	ANDA078212	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1365-1)
68071-3485-3	68071-3485	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20230818	N/A	ANDA	ANDA078212	NuCare Pharmaceuticals,Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3485-3)
51655-388-52	51655-388	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20230519	N/A	ANDA	ANDA078212	Northwind Pharmaceuticals, LLC	BENAZEPRIL HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-388-52)
50090-5751-0	50090-5751	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20210930	N/A	ANDA	ANDA078212	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-5751-0)
50090-5751-2	50090-5751	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20210930	N/A	ANDA	ANDA078212	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5751-2)