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
71335-2186-1	71335-2186	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20221104	N/A	ANDA	ANDA212650	Bryant Ranch Prepack	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2186-1)
71335-2186-2	71335-2186	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20221104	N/A	ANDA	ANDA212650	Bryant Ranch Prepack	RAMELTEON	8 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2186-2)
72189-369-30	72189-369	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20220803	N/A	ANDA	ANDA212650	Direct_Rx	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-369-30)
72162-2176-1	72162-2176	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20231207	N/A	ANDA	ANDA212650	Bryant Ranch Prepack	RAMELTEON	8 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2176-1)
72162-2176-3	72162-2176	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20231207	N/A	ANDA	ANDA212650	Bryant Ranch Prepack	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2176-3)
55700-874-30	55700-874	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20200728	N/A	ANDA	ANDA212650	Quality Care Products, LLC	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-874-30)
80425-0203-1	80425-0203	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20200630	N/A	ANDA	ANDA212650	Advanced Rx Pharmacy of Tennessee, LLC	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0203-1)
52817-235-10	52817-235	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20200630	N/A	ANDA	ANDA212650	TruPharma, LLC	RAMELTEON	8 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52817-235-10)
52817-235-30	52817-235	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20200630	N/A	ANDA	ANDA212650	TruPharma, LLC	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (52817-235-30)
72319-005-01	72319-005	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA212650	i3 Pharmaceuticals, LLC	RAMELTEON	8 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72319-005-01)
72319-005-04	72319-005	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA212650	i3 Pharmaceuticals, LLC	RAMELTEON	8 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72319-005-04)
72319-005-05	72319-005	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET, FILM COATED	ORAL	20200430	N/A	ANDA	ANDA212650	i3 Pharmaceuticals, LLC	RAMELTEON	8 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72319-005-05)