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
71335-2359-3	71335-2359	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20240305	N/A	ANDA	ANDA203245	Bryant Ranch Prepack	AMLODIPINE BESYLATE	5 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (71335-2359-3)
71335-2359-4	71335-2359	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20240305	N/A	ANDA	ANDA203245	Bryant Ranch Prepack	AMLODIPINE BESYLATE	5 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (71335-2359-4)
71335-2359-5	71335-2359	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20240305	N/A	ANDA	ANDA203245	Bryant Ranch Prepack	AMLODIPINE BESYLATE	5 mg/1	180 TABLET in 1 BOTTLE, PLASTIC (71335-2359-5)
71335-2359-6	71335-2359	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20240305	N/A	ANDA	ANDA203245	Bryant Ranch Prepack	AMLODIPINE BESYLATE	5 mg/1	120 TABLET in 1 BOTTLE, PLASTIC (71335-2359-6)
71335-2359-7	71335-2359	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20240305	N/A	ANDA	ANDA203245	Bryant Ranch Prepack	AMLODIPINE BESYLATE	5 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (71335-2359-7)
71335-2359-8	71335-2359	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20240305	N/A	ANDA	ANDA203245	Bryant Ranch Prepack	AMLODIPINE BESYLATE	5 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (71335-2359-8)
71335-2359-9	71335-2359	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20240305	N/A	ANDA	ANDA203245	Bryant Ranch Prepack	AMLODIPINE BESYLATE	5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (71335-2359-9)
68071-2305-2	68071-2305	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20201123	N/A	ANDA	ANDA203245	NuCare Pharmaceuticals,Inc.	AMLODIPINE BESYLATE	10 mg/1	120 TABLET in 1 BOTTLE, PLASTIC (68071-2305-2)
68071-2305-9	68071-2305	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20201123	N/A	ANDA	ANDA203245	NuCare Pharmaceuticals,Inc.	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (68071-2305-9)
29300-396-05	29300-396	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20200622	N/A	ANDA	ANDA203245	Unichem Pharmaceuticals (USA), Inc.	AMLODIPINE BESYLATE	2.5 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (29300-396-05)
29300-396-10	29300-396	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20200622	N/A	ANDA	ANDA203245	Unichem Pharmaceuticals (USA), Inc.	AMLODIPINE BESYLATE	2.5 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (29300-396-10)
29300-396-19	29300-396	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20200622	N/A	ANDA	ANDA203245	Unichem Pharmaceuticals (USA), Inc.	AMLODIPINE BESYLATE	2.5 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (29300-396-19)