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
71335-0078-4	71335-0078	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20220209	N/A	ANDA	ANDA076118	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, COATED in 1 BOTTLE (71335-0078-4)
71335-0078-5	71335-0078	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20220209	N/A	ANDA	ANDA076118	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	20 mg/1	14 TABLET, COATED in 1 BOTTLE (71335-0078-5)
71335-0078-6	71335-0078	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20220209	N/A	ANDA	ANDA076118	Bryant Ranch Prepack	BENAZEPRIL HYDROCHLORIDE	20 mg/1	10 TABLET, COATED in 1 BOTTLE (71335-0078-6)
50090-3243-0	50090-3243	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20171117	N/A	ANDA	ANDA076118	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	20 mg/1	30 TABLET, COATED in 1 BOTTLE (50090-3243-0)
50090-3243-1	50090-3243	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20171103	N/A	ANDA	ANDA076118	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	20 mg/1	90 TABLET, COATED in 1 BOTTLE (50090-3243-1)
63187-499-90	63187-499	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20150202	N/A	ANDA	ANDA076118	Proficient Rx LP	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, COATED in 1 BOTTLE (63187-499-90)
63187-906-30	63187-906	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170901	N/A	ANDA	ANDA076118	Proficient Rx LP	BENAZEPRIL HYDROCHLORIDE	40 mg/1	30 TABLET, COATED in 1 BOTTLE (63187-906-30)
63187-906-60	63187-906	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170901	N/A	ANDA	ANDA076118	Proficient Rx LP	BENAZEPRIL HYDROCHLORIDE	40 mg/1	60 TABLET, COATED in 1 BOTTLE (63187-906-60)
63187-906-90	63187-906	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20170901	N/A	ANDA	ANDA076118	Proficient Rx LP	BENAZEPRIL HYDROCHLORIDE	40 mg/1	90 TABLET, COATED in 1 BOTTLE (63187-906-90)
51407-463-01	51407-463	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20210706	N/A	ANDA	ANDA076118	Golden State Medical Supply, Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	100 TABLET, COATED in 1 BOTTLE (51407-463-01)
51407-463-05	51407-463	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20210706	N/A	ANDA	ANDA076118	Golden State Medical Supply, Inc.	BENAZEPRIL HYDROCHLORIDE	10 mg/1	500 TABLET, COATED in 1 BOTTLE (51407-463-05)
50090-3775-0	50090-3775	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20181105	N/A	ANDA	ANDA076118	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	10 mg/1	30 TABLET, COATED in 1 BOTTLE (50090-3775-0)
50090-3775-2	50090-3775	HUMAN PRESCRIPTION DRUG	Benazepril Hydrochloride	Benazepril Hydrochloride	TABLET, COATED	ORAL	20181105	N/A	ANDA	ANDA076118	A-S Medication Solutions	BENAZEPRIL HYDROCHLORIDE	10 mg/1	90 TABLET, COATED in 1 BOTTLE (50090-3775-2)
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)