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
71610-956-45	71610-956	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20251015	N/A	ANDA	ANDA076719	Aphena Pharma Solutions - Tennessee, LLC	AMLODIPINE BESYLATE	5 mg/1	45 TABLET in 1 BOTTLE (71610-956-45)
51407-950-10	51407-950	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250122	N/A	ANDA	ANDA076719	GSMS, Incorporated	AMLODIPINE BESYLATE	5 mg/1	1000 TABLET in 1 BOTTLE (51407-950-10)
51407-950-90	51407-950	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250122	N/A	ANDA	ANDA076719	GSMS, Incorporated	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE (51407-950-90)
72789-514-95	72789-514	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250626	N/A	ANDA	ANDA076719	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	2.5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (72789-514-95)
51407-951-10	51407-951	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250122	N/A	ANDA	ANDA076719	GSMS, Incorporated	AMLODIPINE BESYLATE	10 mg/1	1000 TABLET in 1 BOTTLE (51407-951-10)
51407-951-90	51407-951	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250122	N/A	ANDA	ANDA076719	GSMS, Incorporated	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE (51407-951-90)
72789-515-30	72789-515	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20251024	N/A	ANDA	ANDA076719	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-515-30)
72789-515-90	72789-515	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20251020	N/A	ANDA	ANDA076719	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (72789-515-90)
72789-515-95	72789-515	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250626	N/A	ANDA	ANDA076719	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (72789-515-95)
71610-928-30	71610-928	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250723	N/A	ANDA	ANDA076719	Aphena Pharma Solutions - Tennessee, LLC	AMLODIPINE BESYLATE	10 mg/1	30 TABLET in 1 BOTTLE (71610-928-30)
71610-928-45	71610-928	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250723	N/A	ANDA	ANDA076719	Aphena Pharma Solutions - Tennessee, LLC	AMLODIPINE BESYLATE	10 mg/1	45 TABLET in 1 BOTTLE (71610-928-45)
71610-928-53	71610-928	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250723	N/A	ANDA	ANDA076719	Aphena Pharma Solutions - Tennessee, LLC	AMLODIPINE BESYLATE	10 mg/1	60 TABLET in 1 BOTTLE (71610-928-53)
72789-516-30	72789-516	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250930	N/A	ANDA	ANDA076719	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	10 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-516-30)
72789-516-90	72789-516	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20251027	N/A	ANDA	ANDA076719	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (72789-516-90)
72789-516-95	72789-516	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20250626	N/A	ANDA	ANDA076719	PD-Rx Pharmaceuticals, Inc.	AMLODIPINE BESYLATE	10 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (72789-516-95)