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
70771-1495-5	70771-1495	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20190723	N/A	ANDA	ANDA211567	Zydus Lifesciences Limited	RAMELTEON	8 mg/1	500 TABLET in 1 BOTTLE (70771-1495-5)
71335-1853-1	71335-1853	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20211221	N/A	ANDA	ANDA211567	Bryant Ranch Prepack	RAMELTEON	8 mg/1	30 TABLET in 1 BOTTLE (71335-1853-1)
70771-1495-3	70771-1495	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20190723	N/A	ANDA	ANDA211567	Zydus Lifesciences Limited	RAMELTEON	8 mg/1	30 TABLET in 1 BOTTLE (70771-1495-3)
70771-1495-1	70771-1495	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20190723	N/A	ANDA	ANDA211567	Zydus Lifesciences Limited	RAMELTEON	8 mg/1	100 TABLET in 1 BOTTLE (70771-1495-1)
76420-628-01	76420-628	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20231017	N/A	ANDA	ANDA211567	Asclemed USA, Inc.	RAMELTEON	8 mg/1	100 TABLET in 1 BOTTLE (76420-628-01)
60687-692-65	60687-692	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20230120	N/A	ANDA	ANDA211567	American Health Packaging	RAMELTEON	8 mg/1	50 BLISTER PACK in 1 CARTON (60687-692-65) / 1 TABLET in 1 BLISTER PACK (60687-692-11)
76420-628-30	76420-628	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20231128	N/A	ANDA	ANDA211567	Asclemed USA, Inc.	RAMELTEON	8 mg/1	30 TABLET in 1 BOTTLE (76420-628-30)
76420-628-60	76420-628	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20231128	N/A	ANDA	ANDA211567	Asclemed USA, Inc.	RAMELTEON	8 mg/1	60 TABLET in 1 BOTTLE (76420-628-60)
76420-628-90	76420-628	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20231128	N/A	ANDA	ANDA211567	Asclemed USA, Inc.	RAMELTEON	8 mg/1	90 TABLET in 1 BOTTLE (76420-628-90)
70710-1344-1	70710-1344	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20190723	N/A	ANDA	ANDA211567	Zydus Pharmaceuticals USA Inc.	RAMELTEON	8 mg/1	100 TABLET in 1 BOTTLE (70710-1344-1)
70710-1344-3	70710-1344	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20190723	N/A	ANDA	ANDA211567	Zydus Pharmaceuticals USA Inc.	RAMELTEON	8 mg/1	30 TABLET in 1 BOTTLE (70710-1344-3)
70710-1344-5	70710-1344	HUMAN PRESCRIPTION DRUG	Ramelteon	Ramelteon	TABLET	ORAL	20190723	N/A	ANDA	ANDA211567	Zydus Pharmaceuticals USA Inc.	RAMELTEON	8 mg/1	500 TABLET in 1 BOTTLE (70710-1344-5)
72189-153-30	72189-153	HUMAN PRESCRIPTION DRUG	RAMELTEON	RAMELTEON	TABLET	ORAL	20201103	N/A	ANDA	ANDA211567	DIRECT RX	RAMELTEON	8 mg/1	30 TABLET in 1 BOTTLE (72189-153-30)