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
68788-7845-6	68788-7845	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20210120	N/A	ANDA	ANDA078212	Preferred Pharmaceuticlas Inc.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7845-6)
68788-7845-8	68788-7845	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20210120	N/A	ANDA	ANDA078212	Preferred Pharmaceuticlas Inc.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (68788-7845-8)
68788-7845-9	68788-7845	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20210120	N/A	ANDA	ANDA078212	Preferred Pharmaceuticlas Inc.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7845-9)
68788-7845-3	68788-7845	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20210120	N/A	ANDA	ANDA078212	Preferred Pharmaceuticlas Inc.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7845-3)
68788-7845-1	68788-7845	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20210120	N/A	ANDA	ANDA078212	Preferred Pharmaceuticlas Inc.	BENAZEPRIL HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-7845-1)
65862-116-90	65862-116	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20080522	N/A	ANDA	ANDA078212	Aurobindo Pharma Limited	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-116-90)
65862-118-01	65862-118	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20080522	N/A	ANDA	ANDA078212	Aurobindo Pharma Limited	BENAZEPRIL HYDROCHLORIDE	40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-118-01)
65862-118-90	65862-118	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20080522	N/A	ANDA	ANDA078212	Aurobindo Pharma Limited	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-118-90)
65862-116-01	65862-116	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20080522	N/A	ANDA	ANDA078212	Aurobindo Pharma Limited	BENAZEPRIL HYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-116-01)
65862-117-01	65862-117	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20080522	N/A	ANDA	ANDA078212	Aurobindo Pharma Limited	BENAZEPRIL HYDROCHLORIDE	20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-117-01)
65862-117-90	65862-117	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20080522	N/A	ANDA	ANDA078212	Aurobindo Pharma Limited	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (65862-117-90)
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)
51655-202-26	51655-202	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20230315	N/A	ANDA	ANDA078212	Northwind Health Company, LLC	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-202-26)
51655-617-26	51655-617	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20220906	N/A	ANDA	ANDA078212	Northwind Health Company, 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 Health Company, LLC	BENAZEPRIL HYDROCHLORIDE	40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-617-52)
51655-388-52	51655-388	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, FILM COATED	ORAL	20230519	N/A	ANDA	ANDA078212	Northwind Health Company, LLC	BENAZEPRIL HYDROCHLORIDE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-388-52)
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)
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)
50090-5750-0	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)