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
72789-261-60	72789-261	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 5 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20230420	N/A	ANDA	ANDA078414	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	5 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (72789-261-60)
72789-261-90	72789-261	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 5 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20220715	N/A	ANDA	ANDA078414	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (72789-261-90)
72789-261-95	72789-261	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 5 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20220715	N/A	ANDA	ANDA078414	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (72789-261-95)
72789-262-30	72789-262	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20230421	N/A	ANDA	ANDA078414	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	10 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-262-30)
72789-262-60	72789-262	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20230421	N/A	ANDA	ANDA078414	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	10 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (72789-262-60)
72789-262-90	72789-262	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20220715	N/A	ANDA	ANDA078414	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (72789-262-90)
72789-262-95	72789-262	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20220715	N/A	ANDA	ANDA078414	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	10 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (72789-262-95)
72789-261-30	72789-261	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 5 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20230420	N/A	ANDA	ANDA078414	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-261-30)
72789-260-95	72789-260	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 2.5 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20220715	N/A	ANDA	ANDA078414	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	2.5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (72789-260-95)
72789-260-90	72789-260	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 2.5 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20220715	N/A	ANDA	ANDA078414	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	2.5 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (72789-260-90)
82804-971-00	82804-971	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20250213	N/A	ANDA	ANDA078414	Proficient Rx LP	AMLODIPINE BESYLATE	10 mg/1	100 TABLET in 1 BOTTLE (82804-971-00)
82804-971-60	82804-971	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20250213	N/A	ANDA	ANDA078414	Proficient Rx LP	AMLODIPINE BESYLATE	10 mg/1	60 TABLET in 1 BOTTLE (82804-971-60)
82804-971-72	82804-971	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20250213	N/A	ANDA	ANDA078414	Proficient Rx LP	AMLODIPINE BESYLATE	10 mg/1	120 TABLET in 1 BOTTLE (82804-971-72)
82804-971-90	82804-971	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20250213	N/A	ANDA	ANDA078414	Proficient Rx LP	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (82804-971-90)
82804-971-11	82804-971	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20250213	N/A	ANDA	ANDA078414	Proficient Rx LP	AMLODIPINE BESYLATE	10 mg/1	1000 TABLET in 1 BOTTLE (82804-971-11)
82804-971-30	82804-971	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20250213	N/A	ANDA	ANDA078414	Proficient Rx LP	AMLODIPINE BESYLATE	10 mg/1	30 TABLET in 1 BOTTLE (82804-971-30)
82804-971-55	82804-971	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20250213	N/A	ANDA	ANDA078414	Proficient Rx LP	AMLODIPINE BESYLATE	10 mg/1	500 TABLET in 1 BOTTLE (82804-971-55)
69584-022-09	69584-022	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 5 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20211001	N/A	ANDA	ANDA078414	Oxford Pharmaceuticals, LLC	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE (69584-022-09)
69584-023-09	69584-023	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20211001	N/A	ANDA	ANDA078414	Oxford Pharmaceuticals, LLC	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (69584-023-09)
69584-023-50	69584-023	HUMAN PRESCRIPTION DRUG	AMLODIPINE BESYLATE 10 mg	AMLODIPINE BESYLATE	TABLET	ORAL	20211001	N/A	ANDA	ANDA078414	Oxford Pharmaceuticals, LLC	AMLODIPINE BESYLATE	10 mg/1	500 TABLET in 1 BOTTLE (69584-023-50)