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
72162-2644-3	72162-2644	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20260507	N/A	ANDA	ANDA215435	Bryant Ranch Prepack	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2644-3)
72162-2644-1	72162-2644	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20260507	N/A	ANDA	ANDA215435	Bryant Ranch Prepack	RAMELTEON	8 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2644-1)
85742-023-23	85742-023	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20260421	N/A	ANDA	ANDA215435	Kanchan Healthcare Inc	RAMELTEON	8 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85742-023-23)
85742-023-22	85742-023	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20260421	N/A	ANDA	ANDA215435	Kanchan Healthcare Inc	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (85742-023-22)