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
71335-2507-8	71335-2507	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20241007	N/A	ANDA	ANDA078043	Bryant Ranch Prepack	AMLODIPINE BESYLATE	10 mg/1	180 TABLET in 1 BOTTLE (71335-2507-8)
71335-2507-9	71335-2507	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20241007	N/A	ANDA	ANDA078043	Bryant Ranch Prepack	AMLODIPINE BESYLATE	10 mg/1	10 TABLET in 1 BOTTLE (71335-2507-9)
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)
68180-720-09	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)
82804-164-90	82804-164	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20241106	N/A	ANDA	ANDA078043	Proficient Rx LP	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (82804-164-90)
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)
68180-233-02	68180-233	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250430	N/A	ANDA	ANDA078043	Lupin Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	2.5 mg/1	1000 TABLET in 1 BOTTLE (68180-233-02)