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
16571-759-01	16571-759	HUMAN PRESCRIPTION DRUG	NATEGLINIDE	NATEGLINIDE	TABLET	ORAL	20201216	N/A	ANDA	ANDA205544	Rising Pharmaceuticals, Inc.	NATEGLINIDE	120 mg/1	100 TABLET in 1 BOTTLE (16571-759-01)
16571-759-09	16571-759	HUMAN PRESCRIPTION DRUG	NATEGLINIDE	NATEGLINIDE	TABLET	ORAL	20201216	N/A	ANDA	ANDA205544	Rising Pharmaceuticals, Inc.	NATEGLINIDE	120 mg/1	90 TABLET in 1 BOTTLE (16571-759-09)
16571-759-50	16571-759	HUMAN PRESCRIPTION DRUG	NATEGLINIDE	NATEGLINIDE	TABLET	ORAL	20201216	N/A	ANDA	ANDA205544	Rising Pharmaceuticals, Inc.	NATEGLINIDE	120 mg/1	500 TABLET in 1 BOTTLE (16571-759-50)
16571-758-50	16571-758	HUMAN PRESCRIPTION DRUG	NATEGLINIDE	NATEGLINIDE	TABLET	ORAL	20201216	N/A	ANDA	ANDA205544	Rising Pharmaceuticals, Inc.	NATEGLINIDE	60 mg/1	500 TABLET in 1 BOTTLE (16571-758-50)
16571-758-09	16571-758	HUMAN PRESCRIPTION DRUG	NATEGLINIDE	NATEGLINIDE	TABLET	ORAL	20201216	N/A	ANDA	ANDA205544	Rising Pharmaceuticals, Inc.	NATEGLINIDE	60 mg/1	90 TABLET in 1 BOTTLE (16571-758-09)
16571-758-01	16571-758	HUMAN PRESCRIPTION DRUG	NATEGLINIDE	NATEGLINIDE	TABLET	ORAL	20201216	N/A	ANDA	ANDA205544	Rising Pharmaceuticals, Inc.	NATEGLINIDE	60 mg/1	100 TABLET in 1 BOTTLE (16571-758-01)