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
24658-798-30	24658-798	HUMAN PRESCRIPTION DRUG	AMINOCAPROIC ACID	AMINOCAPROIC ACID	TABLET	ORAL	20230124	N/A	ANDA	ANDA213928	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	AMINOCAPROIC ACID	500 mg/1	30 TABLET in 1 BOTTLE (24658-798-30)
24658-799-30	24658-799	HUMAN PRESCRIPTION DRUG	AMINOCAPROIC ACID	AMINOCAPROIC ACID	TABLET	ORAL	20230124	N/A	ANDA	ANDA213928	PURACAP LABORATORIES LLC DBA BLU PHARMACEUTICALS	AMINOCAPROIC ACID	1000 mg/1	30 TABLET in 1 BOTTLE (24658-799-30)
80005-128-08	80005-128	HUMAN PRESCRIPTION DRUG	AMINOCAPROIC ACID	AMINOCAPROIC ACID	TABLET	ORAL	20210315	N/A	ANDA	ANDA213928	Carnegie Pharmaceuticals, LLC	AMINOCAPROIC ACID	500 mg/1	30 TABLET in 1 BOTTLE (80005-128-08)
80005-129-08	80005-129	HUMAN PRESCRIPTION DRUG	AMINOCAPROIC ACID	AMINOCAPROIC ACID	TABLET	ORAL	20210315	N/A	ANDA	ANDA213928	Carnegie Pharmaceuticals, LLC	AMINOCAPROIC ACID	1000 mg/1	30 TABLET in 1 BOTTLE (80005-129-08)
70377-102-11	70377-102	HUMAN PRESCRIPTION DRUG	AMINOCAPROIC ACID	AMINOCAPROIC ACID	TABLET	ORAL	20210315	N/A	ANDA	ANDA213928	Biocon Pharma Inc.	AMINOCAPROIC ACID	500 mg/1	30 TABLET in 1 BOTTLE (70377-102-11)
70377-103-11	70377-103	HUMAN PRESCRIPTION DRUG	AMINOCAPROIC ACID	AMINOCAPROIC ACID	TABLET	ORAL	20210315	N/A	ANDA	ANDA213928	Biocon Pharma Inc.	AMINOCAPROIC ACID	1000 mg/1	30 TABLET in 1 BOTTLE (70377-103-11)