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
71205-320-30	71205-320	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA078212	Proficient Rx LP	BENAZEPRIL HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71205-320-30)
71205-320-60	71205-320	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA078212	Proficient Rx LP	BENAZEPRIL HYDROCHLORIDE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71205-320-60)
71205-320-90	71205-320	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20190901	N/A	ANDA	ANDA078212	Proficient Rx LP	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71205-320-90)
50090-3359-0	50090-3359	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20180326	N/A	ANDA	ANDA078212	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-3359-0)
50090-3359-1	50090-3359	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20180202	N/A	ANDA	ANDA078212	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-3359-1)
68071-5028-1	68071-5028	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20190814	N/A	ANDA	ANDA078212	NuCare Pharmaceuticals,Inc.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68071-5028-1)
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)
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)
71335-1365-3	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)
71335-1365-4	71335-1365	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20200311	N/A	ANDA	ANDA078212	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1365-4)
84386-102-01	84386-102	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20260113	N/A	ANDA	ANDA078212	Aurobindo Pharma Limited	BENAZEPRIL HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (84386-102-01)
84386-102-90	84386-102	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20260113	N/A	ANDA	ANDA078212	Aurobindo Pharma Limited	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (84386-102-90)