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）
检索条件:" 注册申请号=ANDA207762"
符合检索条件的记录共 88 条，共 5 页，当前第 2 页 ，可点击列名称排序
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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
70771-1466-1 70771-1466 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1; 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1466-1)
70771-1466-3 70771-1466 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1466-3)
70771-1466-4 70771-1466 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1; 40 mg/1 10 BLISTER PACK in 1 CARTON (70771-1466-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1466-9 70771-1466 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1466-9)
70771-1460-1 70771-1460 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 5 mg/1; 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1460-1)
70771-1460-3 70771-1460 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 5 mg/1; 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1460-3)
70771-1460-4 70771-1460 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 5 mg/1; 10 mg/1 10 BLISTER PACK in 1 CARTON (70771-1460-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1460-9 70771-1460 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 5 mg/1; 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1460-9)
70771-1464-1 70771-1464 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1; 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1464-1)
70771-1464-3 70771-1464 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1; 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1464-3)
70771-1464-4 70771-1464 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1; 10 mg/1 10 BLISTER PACK in 1 CARTON (70771-1464-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1464-9 70771-1464 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 10 mg/1; 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1464-9)
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)
70771-1459-1 70771-1459 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 2.5 mg/1; 40 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (70771-1459-1)
70771-1459-3 70771-1459 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 2.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70771-1459-3)
70771-1459-4 70771-1459 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 2.5 mg/1; 40 mg/1 10 BLISTER PACK in 1 CARTON (70771-1459-4) / 10 TABLET, FILM COATED in 1 BLISTER PACK
70771-1459-9 70771-1459 HUMAN PRESCRIPTION DRUG Amlodipine and atorvastatin Amlodipine and atorvastatin TABLET, FILM COATED ORAL 20190530 N/A ANDA ANDA207762 Zydus Lifesciences Limited AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE 2.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (70771-1459-9)
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