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
58151-065-93	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)
0069-6323-30	0069-6323	HUMAN PRESCRIPTION DRUG	Caduet	amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20220831	N/A	NDA	NDA021540	Pfizer Laboratories Div Pfizer Inc	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-6323-30)
0069-7476-30	0069-7476	HUMAN PRESCRIPTION DRUG	Caduet	amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20220831	N/A	NDA	NDA021540	Pfizer Laboratories Div Pfizer Inc	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1; 80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-7476-30)
66993-266-30	66993-266	HUMAN PRESCRIPTION DRUG	Amlodipine and Atorvastatin	Amlodipine and Atorvastatin	TABLET, COATED	ORAL	20220314	N/A	NDA AUTHORIZED GENERIC	NDA021540	Prasco Laboratories	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 10 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-266-30)
66993-270-30	66993-270	HUMAN PRESCRIPTION DRUG	Amlodipine and Atorvastatin	Amlodipine and Atorvastatin	TABLET, COATED	ORAL	20220314	N/A	NDA AUTHORIZED GENERIC	NDA021540	Prasco Laboratories	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1; 10 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-270-30)