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
69238-2687-1	69238-2687	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine Besylate and Benazepril Hydrochloride	CAPSULE	ORAL	20260414	N/A	ANDA	ANDA077215	Amneal Pharmaceuticals NY LLC	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 20 mg/1	100 CAPSULE in 1 BOTTLE (69238-2687-1)
69238-2684-1	69238-2684	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine Besylate and Benazepril Hydrochloride	CAPSULE	ORAL	20260414	N/A	ANDA	ANDA077215	Amneal Pharmaceuticals NY LLC	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	2.5 mg/1; 10 mg/1	100 CAPSULE in 1 BOTTLE (69238-2684-1)
69238-2685-1	69238-2685	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine Besylate and Benazepril Hydrochloride	CAPSULE	ORAL	20260414	N/A	ANDA	ANDA077215	Amneal Pharmaceuticals NY LLC	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 10 mg/1	100 CAPSULE in 1 BOTTLE (69238-2685-1)
69238-2686-1	69238-2686	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate and Benazepril Hydrochloride	Amlodipine Besylate and Benazepril Hydrochloride	CAPSULE	ORAL	20260414	N/A	ANDA	ANDA077215	Amneal Pharmaceuticals NY LLC	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 20 mg/1	100 CAPSULE in 1 BOTTLE (69238-2686-1)