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)
检索条件:" 注册申请号=ANDA208774"
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
67296-1778-7 67296-1778 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200101 N/A ANDA ANDA208774 RedPharm Drug, Inc. METAXALONE 800 mg/1 15 TABLET in 1 BOTTLE (67296-1778-7)
51655-602-20 51655-602 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20210219 N/A ANDA ANDA208774 Northwind Pharmaceuticals METAXALONE 800 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (51655-602-20)
72789-122-30 72789-122 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200925 N/A ANDA ANDA208774 PD-Rx Pharmaceuticals, Inc. METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (72789-122-30)
64980-472-01 64980-472 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20180924 N/A ANDA ANDA208774 Rising Pharmaceuticals, Inc. METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (64980-472-01)
64980-472-50 64980-472 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20180924 N/A ANDA ANDA208774 Rising Pharmaceuticals, Inc. METAXALONE 800 mg/1 500 TABLET in 1 BOTTLE (64980-472-50)
68788-7499-0 68788-7499 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20191227 N/A ANDA ANDA208774 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 15 TABLET in 1 BOTTLE (68788-7499-0)
68788-7499-1 68788-7499 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20191227 N/A ANDA ANDA208774 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (68788-7499-1)
68788-7499-2 68788-7499 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20191227 N/A ANDA ANDA208774 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 20 TABLET in 1 BOTTLE (68788-7499-2)
68788-7499-3 68788-7499 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20191227 N/A ANDA ANDA208774 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (68788-7499-3)
68788-7499-6 68788-7499 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20191227 N/A ANDA ANDA208774 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (68788-7499-6)
68788-7499-9 68788-7499 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20191227 N/A ANDA ANDA208774 Preferred Pharmaceuticals, Inc. METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (68788-7499-9)
63629-2398-1 63629-2398 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20210223 N/A ANDA ANDA208774 Bryant Ranch Prepack METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (63629-2398-1)
71205-470-30 71205-470 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200824 N/A ANDA ANDA208774 Proficient Rx LP METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (71205-470-30)
71205-470-60 71205-470 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200824 N/A ANDA ANDA208774 Proficient Rx LP METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (71205-470-60)
71205-470-90 71205-470 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20200824 N/A ANDA ANDA208774 Proficient Rx LP METAXALONE 800 mg/1 90 TABLET in 1 BOTTLE (71205-470-90)
72162-1808-1 72162-1808 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20231006 N/A ANDA ANDA208774 Bryant Ranch Prepack METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (72162-1808-1)
45865-161-30 45865-161 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20201209 N/A ANDA ANDA208774 Medsource Pharmaceuticals METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (45865-161-30)
45865-161-60 45865-161 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20210119 N/A ANDA ANDA208774 Medsource Pharmaceuticals METAXALONE 800 mg/1 60 TABLET in 1 BOTTLE (45865-161-60)
71335-1320-0 71335-1320 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20190829 N/A ANDA ANDA208774 Bryant Ranch Prepack METAXALONE 800 mg/1 100 TABLET in 1 BOTTLE (71335-1320-0)
71335-1320-1 71335-1320 HUMAN PRESCRIPTION DRUG Metaxalone Metaxalone TABLET ORAL 20190829 N/A ANDA ANDA208774 Bryant Ranch Prepack METAXALONE 800 mg/1 30 TABLET in 1 BOTTLE (71335-1320-1)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase