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
46708-764-30	46708-764	HUMAN PRESCRIPTION DRUG	Amlodipine and Atorvastatin	Amlodipine and Atorvastatin	TABLET, FILM COATED	ORAL	20250523	N/A	ANDA	ANDA217279	Alembic Pharmaceuticals Limited	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (46708-764-30)
46708-764-90	46708-764	HUMAN PRESCRIPTION DRUG	Amlodipine and Atorvastatin	Amlodipine and Atorvastatin	TABLET, FILM COATED	ORAL	20250523	N/A	ANDA	ANDA217279	Alembic Pharmaceuticals Limited	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	10 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (46708-764-90)
62332-756-30	62332-756	HUMAN PRESCRIPTION DRUG	Amlodipine and Atorvastatin	Amlodipine and Atorvastatin	TABLET, FILM COATED	ORAL	20250523	N/A	ANDA	ANDA217279	Alembic Pharmaceuticals Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	2.5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62332-756-30)
62332-756-90	62332-756	HUMAN PRESCRIPTION DRUG	Amlodipine and Atorvastatin	Amlodipine and Atorvastatin	TABLET, FILM COATED	ORAL	20250523	N/A	ANDA	ANDA217279	Alembic Pharmaceuticals Inc.	AMLODIPINE BESYLATE; ATORVASTATIN CALCIUM TRIHYDRATE	2.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (62332-756-90)