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
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)
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)
66993-263-30	66993-263	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	2.5 mg/1; 10 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-263-30)
66993-267-30	66993-267	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; 20 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-267-30)
66993-271-30	66993-271	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; 20 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-271-30)
0069-6565-30	0069-6565	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; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-6565-30)
0069-7654-30	0069-7654	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; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-7654-30)
66993-264-30	66993-264	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	2.5 mg/1; 20 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-264-30)
66993-268-30	66993-268	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; 40 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-268-30)
66993-272-30	66993-272	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; 40 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-272-30)
0069-6180-30	0069-6180	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; 10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-6180-30)
0069-6747-30	0069-6747	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; 80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-6747-30)
0069-7810-30	0069-7810	HUMAN PRESCRIPTION DRUG	Caduet	amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20220606	N/A	NDA	NDA021540	Pfizer Laboratories Div Pfizer Inc	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1; 10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-7810-30)
66993-265-30	66993-265	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	2.5 mg/1; 40 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-265-30)
66993-269-30	66993-269	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; 80 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-269-30)
66993-273-30	66993-273	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; 80 mg/1	30 TABLET, COATED in 1 BOTTLE (66993-273-30)
0069-2260-30	0069-2260	HUMAN PRESCRIPTION DRUG	Caduet	amlodipine besylate and atorvastatin calcium	TABLET, FILM COATED	ORAL	20040130	N/A	NDA	NDA021540	Pfizer Laboratories Div Pfizer Inc	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-2260-30)
0069-7232-30	0069-7232	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; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0069-7232-30)