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
51655-869-83	51655-869	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20231221	N/A	ANDA	ANDA077073	Northwind Pharmaceuticals, LLC	AMLODIPINE BESYLATE	10 mg/1	180 TABLET in 1 BOTTLE, PLASTIC (51655-869-83)
70518-0297-0	70518-0297	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20170308	N/A	ANDA	ANDA077073	REMEDYREPACK INC.	AMLODIPINE BESYLATE	10 mg/1	30 TABLET in 1 BLISTER PACK (70518-0297-0)
70518-0297-1	70518-0297	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20170424	N/A	ANDA	ANDA077073	REMEDYREPACK INC.	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-0297-1)
43063-764-30	43063-764	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20170508	N/A	ANDA	ANDA077073	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	2.5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (43063-764-30)
82009-026-10	82009-026	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20231215	N/A	ANDA	ANDA077073	Quallent Pharmaceuticals Health LLC	AMLODIPINE BESYLATE	2.5 mg/1	1000 TABLET in 1 BOTTLE (82009-026-10)
51655-044-52	51655-044	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20231130	N/A	ANDA	ANDA077073	Northwind Pharmaceuticals, LLC	AMLODIPINE BESYLATE	5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-044-52)
69097-128-05	69097-128	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20070926	N/A	ANDA	ANDA077073	Cipla USA Inc.	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (69097-128-05)
69097-128-15	69097-128	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20070926	N/A	ANDA	ANDA077073	Cipla USA Inc.	AMLODIPINE BESYLATE	10 mg/1	1000 TABLET in 1 BOTTLE (69097-128-15)