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
52605-041-10	52605-041	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20160711	N/A	ANDA	ANDA207821	POLYGEN PHARMACEUTICALS INC.	AMLODIPINE BESYLATE	2.5 mg/1	1000 TABLET in 1 BOTTLE (52605-041-10)
52605-041-19	52605-041	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20160711	N/A	ANDA	ANDA207821	POLYGEN PHARMACEUTICALS INC.	AMLODIPINE BESYLATE	2.5 mg/1	90 TABLET in 1 BOTTLE (52605-041-19)
52605-042-10	52605-042	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20160711	N/A	ANDA	ANDA207821	POLYGEN PHARMACEUTICALS INC.	AMLODIPINE BESYLATE	5 mg/1	1000 TABLET in 1 BOTTLE (52605-042-10)
52605-042-19	52605-042	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20160711	N/A	ANDA	ANDA207821	POLYGEN PHARMACEUTICALS INC.	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE (52605-042-19)
52605-043-10	52605-043	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20160711	N/A	ANDA	ANDA207821	POLYGEN PHARMACEUTICALS INC.	AMLODIPINE BESYLATE	10 mg/1	1000 TABLET in 1 BOTTLE (52605-043-10)
52605-043-19	52605-043	HUMAN PRESCRIPTION DRUG	amlodipine besylate	amlodipine besylate	TABLET	ORAL	20160711	N/A	ANDA	ANDA207821	POLYGEN PHARMACEUTICALS INC.	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (52605-043-19)