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
63629-8531-1	63629-8531	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20201001	N/A	ANDA	ANDA213186	Bryant Ranch Prepack	RAMELTEON	8 mg/1	30 TABLET in 1 BOTTLE (63629-8531-1)
42291-776-30	42291-776	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20201221	N/A	ANDA	ANDA213186	AvKARE	RAMELTEON	8 mg/1	30 TABLET in 1 BOTTLE (42291-776-30)
71205-918-00	71205-918	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20210707	N/A	ANDA	ANDA213186	Proficient Rx LP	RAMELTEON	8 mg/1	100 TABLET in 1 BOTTLE (71205-918-00)
71205-918-30	71205-918	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20210707	N/A	ANDA	ANDA213186	Proficient Rx LP	RAMELTEON	8 mg/1	30 TABLET in 1 BOTTLE (71205-918-30)
71205-918-55	71205-918	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20210707	N/A	ANDA	ANDA213186	Proficient Rx LP	RAMELTEON	8 mg/1	500 TABLET in 1 BOTTLE (71205-918-55)
71205-918-60	71205-918	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20210707	N/A	ANDA	ANDA213186	Proficient Rx LP	RAMELTEON	8 mg/1	60 TABLET in 1 BOTTLE (71205-918-60)
71205-918-72	71205-918	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20210707	N/A	ANDA	ANDA213186	Proficient Rx LP	RAMELTEON	8 mg/1	120 TABLET in 1 BOTTLE (71205-918-72)
71205-918-90	71205-918	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20210707	N/A	ANDA	ANDA213186	Proficient Rx LP	RAMELTEON	8 mg/1	90 TABLET in 1 BOTTLE (71205-918-90)
70010-028-01	70010-028	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20230515	N/A	ANDA	ANDA213186	Granules Pharmaceuticals Inc.	RAMELTEON	8 mg/1	100 TABLET in 1 BOTTLE (70010-028-01)
70010-028-03	70010-028	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20201001	N/A	ANDA	ANDA213186	Granules Pharmaceuticals Inc.	RAMELTEON	8 mg/1	30 TABLET in 1 BOTTLE (70010-028-03)
70010-028-05	70010-028	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20201001	N/A	ANDA	ANDA213186	Granules Pharmaceuticals Inc.	RAMELTEON	8 mg/1	500 TABLET in 1 BOTTLE (70010-028-05)