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
68788-6957-9	68788-6957	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170502	N/A	ANDA	ANDA076118	Preferred Pharmaceuticals Inc.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, COATED in 1 BOTTLE (68788-6957-9)
51655-065-26	51655-065	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20220527	N/A	ANDA	ANDA076118	Northwind Health Company, LLC	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-065-26)
51655-065-52	51655-065	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20160623	N/A	ANDA	ANDA076118	Northwind Health Company, LLC	BENAZEPRIL HYDROCHLORIDE	10 mg/1	30 TABLET, COATED in 1 BOTTLE (51655-065-52)
71335-0267-1	71335-0267	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20220209	N/A	ANDA	ANDA076118	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	40 mg/1	30 TABLET, COATED in 1 BOTTLE (71335-0267-1)
71335-0267-2	71335-0267	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20220209	N/A	ANDA	ANDA076118	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	40 mg/1	100 TABLET, COATED in 1 BOTTLE (71335-0267-2)
71335-0267-3	71335-0267	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20220209	N/A	ANDA	ANDA076118	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	40 mg/1	60 TABLET, COATED in 1 BOTTLE (71335-0267-3)
68071-5130-0	68071-5130	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20191212	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals,Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	100 TABLET, COATED in 1 BOTTLE (68071-5130-0)
43547-338-03	43547-338	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20190630	N/A	ANDA	ANDA076118	Solco healthcare U.S., LLC	BENAZEPRIL HYDROCHLORIDE	40 mg/1	30 TABLET, COATED in 1 BOTTLE (43547-338-03)
43547-338-10	43547-338	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20140101	N/A	ANDA	ANDA076118	Solco healthcare U.S., LLC	BENAZEPRIL HYDROCHLORIDE	40 mg/1	100 TABLET, COATED in 1 BOTTLE (43547-338-10)
43547-338-50	43547-338	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20140101	N/A	ANDA	ANDA076118	Solco healthcare U.S., LLC	BENAZEPRIL HYDROCHLORIDE	40 mg/1	500 TABLET, COATED in 1 BOTTLE (43547-338-50)
68071-1769-1	68071-1769	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20191018	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals,Inc.	BENAZEPRIL HYDROCHLORIDE	20 mg/1	100 TABLET, COATED in 1 BOTTLE (68071-1769-1)
68071-3324-1	68071-3324	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170710	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	120 TABLET, COATED in 1 BOTTLE (68071-3324-1)
68071-3324-3	68071-3324	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170710	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	30 TABLET, COATED in 1 BOTTLE (68071-3324-3)
68071-3324-6	68071-3324	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170710	N/A	ANDA	ANDA076118	NuCare Pharmaceuticals, Inc.	BENAZEPRIL HYDROCHLORIDE	5 mg/1	60 TABLET, COATED in 1 BOTTLE (68071-3324-6)
71335-0267-4	71335-0267	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20220209	N/A	ANDA	ANDA076118	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, COATED in 1 BOTTLE (71335-0267-4)