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
0078-0405-05	0078-0405	HUMAN PRESCRIPTION DRUG	Lotrel	amlodipine besylate and benazepril hydrochloride	CAPSULE	ORAL	19950303	20260930	NDA	NDA020364	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 10 mg/1	100 CAPSULE in 1 BOTTLE (0078-0405-05)
0078-0406-05	0078-0406	HUMAN PRESCRIPTION DRUG	Lotrel	amlodipine besylate and benazepril hydrochloride	CAPSULE	ORAL	19950303	20260331	NDA	NDA020364	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	5 mg/1; 20 mg/1	100 CAPSULE in 1 BOTTLE (0078-0406-05)
0078-0379-05	0078-0379	HUMAN PRESCRIPTION DRUG	Lotrel	amlodipine besylate and benazepril hydrochloride	CAPSULE	ORAL	19950303	20260731	NDA	NDA020364	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 40 mg/1	100 CAPSULE in 1 BOTTLE (0078-0379-05)
0078-0364-05	0078-0364	HUMAN PRESCRIPTION DRUG	Lotrel	amlodipine besylate and benazepril hydrochloride	CAPSULE	ORAL	19950303	20260331	NDA	NDA020364	Novartis Pharmaceuticals Corporation	AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE	10 mg/1; 20 mg/1	100 CAPSULE in 1 BOTTLE (0078-0364-05)