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
71335-2411-1	71335-2411	HUMAN PRESCRIPTION DRUG	RAMELTEON	RAMELTEON	TABLET, FILM COATED	ORAL	20240610	N/A	ANDA	ANDA215972	Bryant Ranch Prepack	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2411-1)
71335-2411-2	71335-2411	HUMAN PRESCRIPTION DRUG	RAMELTEON	RAMELTEON	TABLET, FILM COATED	ORAL	20240610	N/A	ANDA	ANDA215972	Bryant Ranch Prepack	RAMELTEON	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2411-2)
76420-880-01	76420-880	HUMAN PRESCRIPTION DRUG	RAMELTEON	RAMELTEON	TABLET, FILM COATED	ORAL	20250117	N/A	ANDA	ANDA215972	Asclemed USA, Inc.	RAMELTEON	8 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76420-880-01)
76420-880-30	76420-880	HUMAN PRESCRIPTION DRUG	RAMELTEON	RAMELTEON	TABLET, FILM COATED	ORAL	20250117	N/A	ANDA	ANDA215972	Asclemed USA, Inc.	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-880-30)
76420-880-60	76420-880	HUMAN PRESCRIPTION DRUG	RAMELTEON	RAMELTEON	TABLET, FILM COATED	ORAL	20250117	N/A	ANDA	ANDA215972	Asclemed USA, Inc.	RAMELTEON	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-880-60)
76420-880-90	76420-880	HUMAN PRESCRIPTION DRUG	RAMELTEON	RAMELTEON	TABLET, FILM COATED	ORAL	20250117	N/A	ANDA	ANDA215972	Asclemed USA, Inc.	RAMELTEON	8 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (76420-880-90)
59651-505-01	59651-505	HUMAN PRESCRIPTION DRUG	RAMELTEON	RAMELTEON	TABLET, FILM COATED	ORAL	20230710	N/A	ANDA	ANDA215972	Aurobindo Pharma Limited	RAMELTEON	8 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-505-01)
59651-505-30	59651-505	HUMAN PRESCRIPTION DRUG	RAMELTEON	RAMELTEON	TABLET, FILM COATED	ORAL	20230710	N/A	ANDA	ANDA215972	Aurobindo Pharma Limited	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-505-30)