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
63187-914-60	63187-914	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20171002	N/A	ANDA	ANDA077073	Proficient Rx LP	AMLODIPINE BESYLATE	10 mg/1	60 TABLET in 1 BOTTLE (63187-914-60)
63187-914-90	63187-914	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20171002	N/A	ANDA	ANDA077073	Proficient Rx LP	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (63187-914-90)
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)
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)
71335-0218-8	71335-0218	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20220923	N/A	ANDA	ANDA077073	Bryant Ranch Prepack	AMLODIPINE BESYLATE	10 mg/1	180 TABLET in 1 BOTTLE (71335-0218-8)
71335-0218-9	71335-0218	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20220923	N/A	ANDA	ANDA077073	Bryant Ranch Prepack	AMLODIPINE BESYLATE	10 mg/1	10 TABLET in 1 BOTTLE (71335-0218-9)
70518-0835-3	70518-0835	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20230608	N/A	ANDA	ANDA077073	REMEDYREPACK INC.	AMLODIPINE BESYLATE	5 mg/1	30 TABLET in 1 BLISTER PACK (70518-0835-3)
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)
69097-126-15	69097-126	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20070926	N/A	ANDA	ANDA077073	Cipla USA Inc.	AMLODIPINE BESYLATE	2.5 mg/1	1000 TABLET in 1 BOTTLE (69097-126-15)
82009-027-10	82009-027	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20221201	N/A	ANDA	ANDA077073	Quallent Pharmaceuticals Health LLC	AMLODIPINE BESYLATE	5 mg/1	1000 TABLET in 1 BOTTLE (82009-027-10)
51655-044-52	51655-044	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20231130	N/A	ANDA	ANDA077073	Northwind Health Company, LLC	AMLODIPINE BESYLATE	5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-044-52)
69097-127-05	69097-127	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20070926	N/A	ANDA	ANDA077073	Cipla USA Inc.	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE (69097-127-05)
69097-127-15	69097-127	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20070926	N/A	ANDA	ANDA077073	Cipla USA Inc.	AMLODIPINE BESYLATE	5 mg/1	1000 TABLET in 1 BOTTLE (69097-127-15)
82009-028-10	82009-028	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE	AMLODIPINE BESYLATE	TABLET	ORAL	20221201	N/A	ANDA	ANDA077073	Quallent Pharmaceuticals Health LLC	AMLODIPINE BESYLATE	10 mg/1	1000 TABLET in 1 BOTTLE (82009-028-10)