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
68001-132-00	68001-132	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine Besylate and Benazepril Hydrochloride	CAPSULE	ORAL	20150716	N/A	ANDA	ANDA078466	BluePoint Laboratories	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	2.5 mg/1; 10 mg/1	100 CAPSULE in 1 BOTTLE (68001-132-00)
68001-133-00	68001-133	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine Besylate and Benazepril Hydrochloride	CAPSULE	ORAL	20150716	N/A	ANDA	ANDA078466	BluePoint Laboratories	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 10 mg/1	100 CAPSULE in 1 BOTTLE (68001-133-00)
70518-2566-0	70518-2566	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine Besylate and Benazepril Hydrochloride	CAPSULE	ORAL	20200204	N/A	ANDA	ANDA078466	REMEDYREPACK INC.	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 20 mg/1	90 CAPSULE in 1 BOTTLE, PLASTIC (70518-2566-0)