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
51407-523-01	51407-523	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20240829	N/A	ANDA	ANDA216209	Golden State Medical Supply, Inc.	RAMELTEON	8 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (51407-523-01)
51407-523-30	51407-523	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20240829	N/A	ANDA	ANDA216209	Golden State Medical Supply, Inc.	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (51407-523-30)
70700-272-05	70700-272	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20221125	N/A	ANDA	ANDA216209	Xiromed, LLC	RAMELTEON	8 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (70700-272-05)
70700-272-10	70700-272	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20221125	N/A	ANDA	ANDA216209	Xiromed, LLC	RAMELTEON	8 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (70700-272-10)
70700-272-30	70700-272	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20221125	N/A	ANDA	ANDA216209	Xiromed, LLC	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70700-272-30)