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
58151-062-93	58151-062	HUMAN PRESCRIPTION DRUG	Caduet	amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20260225	N/A	NDA	NDA021540	Viatris Specialty LLC	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (58151-062-93)
58151-067-93	58151-067	HUMAN PRESCRIPTION DRUG	Caduet	amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20260226	N/A	NDA	NDA021540	Viatris Specialty LLC	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (58151-067-93)
58151-063-93	58151-063	HUMAN PRESCRIPTION DRUG	Caduet	amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20260225	N/A	NDA	NDA021540	Viatris Specialty LLC	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1; 80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (58151-063-93)
58151-065-93	58151-065	HUMAN PRESCRIPTION DRUG	Caduet	amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20260225	N/A	NDA	NDA021540	Viatris Specialty LLC	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (58151-065-93)
58151-066-93	58151-066	HUMAN PRESCRIPTION DRUG	Caduet	amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20260226	N/A	NDA	NDA021540	Viatris Specialty LLC	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (58151-066-93)