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
68382-424-01	68382-424	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	2.5 mg/1; 10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-424-01)
68382-424-06	68382-424	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	2.5 mg/1; 10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-424-06)
68382-424-16	68382-424	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	2.5 mg/1; 10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-424-16)
68382-424-77	68382-424	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	2.5 mg/1; 10 mg/1	10 BLISTER PACK in 1 CARTON (68382-424-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-424-30)
68382-428-01	68382-428	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 20 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-428-01)
68382-428-06	68382-428	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-428-06)
68382-428-16	68382-428	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-428-16)
68382-426-01	68382-426	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	2.5 mg/1; 40 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-426-01)
68382-426-06	68382-426	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	2.5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-426-06)
68382-426-16	68382-426	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	2.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-426-16)
68382-426-77	68382-426	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	2.5 mg/1; 40 mg/1	10 BLISTER PACK in 1 CARTON (68382-426-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-426-30)
68382-430-01	68382-430	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 80 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-430-01)
68382-430-06	68382-430	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 80 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-430-06)
68382-430-16	68382-430	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 80 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-430-16)
68382-427-01	68382-427	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-427-01)
68382-427-06	68382-427	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-427-06)
68382-427-16	68382-427	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68382-427-16)
68382-427-77	68382-427	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	5 mg/1; 10 mg/1	10 BLISTER PACK in 1 CARTON (68382-427-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68382-427-30)
68382-431-01	68382-431	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1; 10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68382-431-01)
68382-431-06	68382-431	HUMAN PRESCRIPTION DRUG	Amlodipine and atorvastatin	Amlodipine and atorvastatin	TABLET, FILM COATED	ORAL	20190530	N/A	ANDA	ANDA207762	Zydus Pharmaceuticals (USA) Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1; 10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68382-431-06)