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
63629-7535-2	63629-7535	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20240708	N/A	ANDA	ANDA202239	Bryant Ranch Prepack	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 20 mg/1	60 CAPSULE in 1 BOTTLE (63629-7535-2)
63629-7535-3	63629-7535	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20180622	N/A	ANDA	ANDA202239	Bryant Ranch Prepack	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 20 mg/1	90 CAPSULE in 1 BOTTLE (63629-7535-3)
65862-585-01	65862-585	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20120905	N/A	ANDA	ANDA202239	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 40 mg/1	100 CAPSULE in 1 BOTTLE (65862-585-01)
65862-585-05	65862-585	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20120905	N/A	ANDA	ANDA202239	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 40 mg/1	500 CAPSULE in 1 BOTTLE (65862-585-05)
70518-1928-0	70518-1928	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20190301	N/A	ANDA	ANDA202239	REMEDYREPACK INC.	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 10 mg/1	90 CAPSULE in 1 BOTTLE, PLASTIC (70518-1928-0)
51655-213-26	51655-213	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20221020	N/A	ANDA	ANDA202239	Northwind Health Company, LLC	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 20 mg/1	90 CAPSULE in 1 BOTTLE, PLASTIC (51655-213-26)
51655-213-52	51655-213	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20230502	N/A	ANDA	ANDA202239	Northwind Health Company, LLC	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 20 mg/1	30 CAPSULE in 1 BOTTLE, PLASTIC (51655-213-52)
50090-4284-0	50090-4284	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20190429	N/A	ANDA	ANDA202239	A-S Medication Solutions	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 20 mg/1	30 CAPSULE in 1 BOTTLE (50090-4284-0)
50090-4284-1	50090-4284	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20190429	N/A	ANDA	ANDA202239	A-S Medication Solutions	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 20 mg/1	90 CAPSULE in 1 BOTTLE (50090-4284-1)
65862-583-05	65862-583	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20120905	N/A	ANDA	ANDA202239	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 10 mg/1	500 CAPSULE in 1 BOTTLE (65862-583-05)
65862-583-01	65862-583	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20120905	N/A	ANDA	ANDA202239	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 10 mg/1	100 CAPSULE in 1 BOTTLE (65862-583-01)
65862-587-01	65862-587	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20120905	N/A	ANDA	ANDA202239	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 40 mg/1	100 CAPSULE in 1 BOTTLE (65862-587-01)
65862-587-05	65862-587	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20120905	N/A	ANDA	ANDA202239	Aurobindo Pharma Limited	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 40 mg/1	500 CAPSULE in 1 BOTTLE (65862-587-05)