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
72162-2161-3	72162-2161	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20231207	N/A	ANDA	ANDA213815	Bryant Ranch Prepack	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72162-2161-3)
72189-484-30	72189-484	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20230601	N/A	ANDA	ANDA213815	Direct_Rx	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-484-30)
80425-0343-1	80425-0343	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20230615	N/A	ANDA	ANDA213815	Advanced Rx Pharmacy of Tennessee, LLC	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0343-1)
0832-1250-11	0832-1250	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20201026	N/A	ANDA	ANDA213815	Upsher-Smith Laboratories, LLC	RAMELTEON	8 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0832-1250-11)
0832-1250-30	0832-1250	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20201026	N/A	ANDA	ANDA213815	Upsher-Smith Laboratories, LLC	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0832-1250-30)