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
23155-925-01	23155-925	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20251015	N/A	ANDA	ANDA091431	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 40 mg/1	100 CAPSULE in 1 BOTTLE (23155-925-01)
23155-925-05	23155-925	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20251015	N/A	ANDA	ANDA091431	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 40 mg/1	500 CAPSULE in 1 BOTTLE (23155-925-05)
23155-925-10	23155-925	HUMAN PRESCRIPTION DRUG	Amlodipine and Benazepril Hydrochloride	Amlodipine and Benazepril Hydrochloride	CAPSULE	ORAL	20251015	N/A	ANDA	ANDA091431	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 40 mg/1	1000 CAPSULE in 1 BOTTLE (23155-925-10)