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
72241-003-04	72241-003	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, COATED	ORAL	20210819	N/A	ANDA	ANDA206432	Modavar Pharmaceuticals LLC	NATEGLINIDE	120 mg/1	90 TABLET, COATED in 1 BOTTLE (72241-003-04)
72241-003-05	72241-003	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, COATED	ORAL	20210819	N/A	ANDA	ANDA206432	Modavar Pharmaceuticals LLC	NATEGLINIDE	120 mg/1	100 TABLET, COATED in 1 BOTTLE (72241-003-05)
72241-002-04	72241-002	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, COATED	ORAL	20210819	N/A	ANDA	ANDA206432	Modavar Pharmaceuticals LLC	NATEGLINIDE	60 mg/1	90 TABLET, COATED in 1 BOTTLE (72241-002-04)
72241-002-05	72241-002	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, COATED	ORAL	20210819	N/A	ANDA	ANDA206432	Modavar Pharmaceuticals LLC	NATEGLINIDE	60 mg/1	100 TABLET, COATED in 1 BOTTLE (72241-002-05)
71209-031-04	71209-031	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, COATED	ORAL	20201217	N/A	ANDA	ANDA206432	Cadila Pharmaceuticals Limited	NATEGLINIDE	120 mg/1	90 TABLET, COATED in 1 BOTTLE (71209-031-04)
71209-031-05	71209-031	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, COATED	ORAL	20140210	N/A	ANDA	ANDA206432	Cadila Pharmaceuticals Limited	NATEGLINIDE	120 mg/1	100 TABLET, COATED in 1 BOTTLE (71209-031-05)
75834-206-01	75834-206	HUMAN PRESCRIPTION DRUG	NATEGLINIDE	NATEGLINIDE	TABLET, COATED	ORAL	20190925	N/A	ANDA	ANDA206432	Nivagen Pharmaceuticals, Inc.	NATEGLINIDE	120 mg/1	100 TABLET, COATED in 1 BOTTLE (75834-206-01)
71209-030-04	71209-030	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, COATED	ORAL	20201217	N/A	ANDA	ANDA206432	Cadila Pharmaceuticals Limited	NATEGLINIDE	60 mg/1	90 TABLET, COATED in 1 BOTTLE (71209-030-04)
71209-030-05	71209-030	HUMAN PRESCRIPTION DRUG	Nateglinide	Nateglinide	TABLET, COATED	ORAL	20140210	N/A	ANDA	ANDA206432	Cadila Pharmaceuticals Limited	NATEGLINIDE	60 mg/1	100 TABLET, COATED in 1 BOTTLE (71209-030-05)
75834-205-01	75834-205	HUMAN PRESCRIPTION DRUG	NATEGLINIDE	NATEGLINIDE	TABLET, COATED	ORAL	20190925	N/A	ANDA	ANDA206432	Nivagen Pharmaceuticals, Inc.	NATEGLINIDE	60 mg/1	100 TABLET, COATED in 1 BOTTLE (75834-205-01)