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
68788-7985-6	68788-7985	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20210806	N/A	ANDA	ANDA078925	Preferred Pharmaceuticals Inc.	AMLODIPINE BESYLATE	10 mg/1	60 TABLET in 1 BOTTLE (68788-7985-6)
68788-7985-9	68788-7985	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20210806	N/A	ANDA	ANDA078925	Preferred Pharmaceuticals Inc.	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (68788-7985-9)
70518-2632-0	70518-2632	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20200317	N/A	ANDA	ANDA078925	REMEDYREPACK INC.	AMLODIPINE BESYLATE	10 mg/1	30 TABLET in 1 BLISTER PACK (70518-2632-0)
70518-2632-5	70518-2632	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20250609	N/A	ANDA	ANDA078925	REMEDYREPACK INC.	AMLODIPINE BESYLATE	10 mg/1	30 TABLET in 1 BLISTER PACK (70518-2632-5)
60760-614-30	60760-614	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20210923	N/A	ANDA	ANDA078925	St. Mary's Medical Park Pharmacy	AMLODIPINE BESYLATE	10 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (60760-614-30)
51655-291-26	51655-291	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20230403	N/A	ANDA	ANDA078925	Northwind Health Company, LLC	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (51655-291-26)
51655-291-52	51655-291	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20221027	N/A	ANDA	ANDA078925	Northwind Health Company, LLC	AMLODIPINE BESYLATE	5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-291-52)
50090-5059-0	50090-5059	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20200526	N/A	ANDA	ANDA078925	A-S Medication Solutions	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE (50090-5059-0)
67877-900-90	67877-900	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20251206	N/A	ANDA	ANDA078925	Ascend Laboratories, LLC	AMLODIPINE BESYLATE	2.5 mg/1	90 TABLET in 1 BOTTLE (67877-900-90)
60687-496-01	60687-496	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20190822	N/A	ANDA	ANDA078925	American Health Packaging	AMLODIPINE BESYLATE	10 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-496-01) / 1 TABLET in 1 BLISTER PACK (60687-496-11)
50090-2581-0	50090-2581	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20161108	N/A	ANDA	ANDA078925	A-S Medication Solutions	AMLODIPINE BESYLATE	10 mg/1	30 TABLET in 1 BOTTLE (50090-2581-0)
50090-2581-1	50090-2581	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20161101	N/A	ANDA	ANDA078925	A-S Medication Solutions	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (50090-2581-1)
50090-2581-2	50090-2581	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20230713	N/A	ANDA	ANDA078925	A-S Medication Solutions	AMLODIPINE BESYLATE	10 mg/1	100 TABLET in 1 BOTTLE (50090-2581-2)
71205-596-30	71205-596	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20210729	N/A	ANDA	ANDA078925	Proficient Rx LP	AMLODIPINE BESYLATE	5 mg/1	30 TABLET in 1 BOTTLE (71205-596-30)
71205-596-60	71205-596	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20210729	N/A	ANDA	ANDA078925	Proficient Rx LP	AMLODIPINE BESYLATE	5 mg/1	60 TABLET in 1 BOTTLE (71205-596-60)
71205-596-90	71205-596	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine besylate	TABLET	ORAL	20210729	N/A	ANDA	ANDA078925	Proficient Rx LP	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE (71205-596-90)