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
49411-051-30	49411-051	HUMAN PRESCRIPTION DRUG	AMICAR	Aminocaproic Acid	TABLET	ORAL	20150601	N/A	NDA	NDA015197	Akorn Operating Company LLC	AMINOCAPROIC ACID	1000 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (49411-051-30)
17478-769-30	17478-769	HUMAN PRESCRIPTION DRUG	Aminocaproic Acid	Aminocaproic Acid	TABLET	ORAL	20190312	N/A	NDA AUTHORIZED GENERIC	NDA015197	Akorn Operating Company LLC	AMINOCAPROIC ACID	1000 mg/1	30 TABLET in 1 BOTTLE (17478-769-30)
17478-768-30	17478-768	HUMAN PRESCRIPTION DRUG	Aminocaproic Acid	Aminocaproic Acid	TABLET	ORAL	20190312	N/A	NDA AUTHORIZED GENERIC	NDA015197	Akorn Operating Company LLC	AMINOCAPROIC ACID	500 mg/1	30 TABLET in 1 BOTTLE (17478-768-30)
49411-050-30	49411-050	HUMAN PRESCRIPTION DRUG	AMICAR	Aminocaproic Acid	TABLET	ORAL	20150601	N/A	NDA	NDA015197	Akorn Operating Company LLC	AMINOCAPROIC ACID	500 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (49411-050-30)
0054-1110-13	0054-1110	HUMAN PRESCRIPTION DRUG	Aminocaproic Acid	Aminocaproic Acid	TABLET	ORAL	20241112	N/A	NDA AUTHORIZED GENERIC	NDA015197	Hikma Pharmaceuticals USA Inc.	AMINOCAPROIC ACID	1000 mg/1	30 TABLET in 1 BOTTLE (0054-1110-13)