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
29300-398-05	29300-398	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20200622	N/A	ANDA	ANDA203245	Unichem Pharmaceuticals (USA), Inc.	AMLODIPINE BESYLATE	10 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (29300-398-05)
29300-398-10	29300-398	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20200622	N/A	ANDA	ANDA203245	Unichem Pharmaceuticals (USA), Inc.	AMLODIPINE BESYLATE	10 mg/1	1000 TABLET in 1 BOTTLE, PLASTIC (29300-398-10)
29300-398-19	29300-398	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20200622	N/A	ANDA	ANDA203245	Unichem Pharmaceuticals (USA), Inc.	AMLODIPINE BESYLATE	10 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (29300-398-19)
72189-520-30	72189-520	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20231103	N/A	ANDA	ANDA203245	Direct_Rx	AMLODIPINE BESYLATE	5 mg/1	30 TABLET in 1 BOTTLE (72189-520-30)
72189-520-90	72189-520	HUMAN PRESCRIPTION DRUG	Amlodipine Besylate	Amlodipine Besylate	TABLET	ORAL	20231103	N/A	ANDA	ANDA203245	Direct_Rx	AMLODIPINE BESYLATE	5 mg/1	90 TABLET in 1 BOTTLE (72189-520-90)
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)