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
68180-720-09	68180-720	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20180815	20251231	ANDA	ANDA078043	Lupin Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE (68180-720-09)
68180-721-03	68180-721	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20181023	N/A	ANDA	ANDA078043	Lupin Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	10 mg/1	1000 TABLET in 1 BOTTLE (68180-721-03)
68180-721-09	68180-721	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20180815	N/A	ANDA	ANDA078043	Lupin Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (68180-721-09)
68180-720-03	68180-720	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20181031	20260131	ANDA	ANDA078043	Lupin Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	5 mg/1	1000 TABLET in 1 BOTTLE (68180-720-03)
68180-719-09	68180-719	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20181031	20260131	ANDA	ANDA078043	Lupin Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	2.5 mg/1	90 TABLET in 1 BOTTLE (68180-719-09)
68180-233-01	68180-233	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20240411	N/A	ANDA	ANDA078043	Lupin Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	2.5 mg/1	90 TABLET in 1 BOTTLE (68180-233-01)