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=ANDA040489"
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
45865-242-30 45865-242 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20240205 N/A ANDA ANDA040489 Medsource Pharmaceuticals METHOCARBAMOL 500 mg/1 30 TABLET in 1 BOTTLE (45865-242-30)
45865-242-60 45865-242 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20230208 N/A ANDA ANDA040489 Medsource Pharmaceuticals METHOCARBAMOL 500 mg/1 60 TABLET in 1 BOTTLE (45865-242-60)
76420-626-01 76420-626 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20231017 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 100 TABLET in 1 BOTTLE (76420-626-01)
76420-626-30 76420-626 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20231017 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 30 TABLET in 1 BOTTLE (76420-626-30)
76420-626-60 76420-626 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20231017 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 60 TABLET in 1 BOTTLE (76420-626-60)
76420-626-90 76420-626 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20231017 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 90 TABLET in 1 BOTTLE (76420-626-90)
76420-638-01 76420-638 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20231017 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 100 TABLET in 1 BOTTLE (76420-638-01)
76420-638-30 76420-638 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20231017 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 30 TABLET in 1 BOTTLE (76420-638-30)
76420-638-60 76420-638 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20231017 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 60 TABLET in 1 BOTTLE (76420-638-60)
76420-638-90 76420-638 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20231017 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 90 TABLET in 1 BOTTLE (76420-638-90)
76420-258-10 76420-258 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 100 TABLET in 1 BOTTLE (76420-258-10)
76420-258-30 76420-258 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 30 TABLET in 1 BOTTLE (76420-258-30)
76420-258-60 76420-258 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 60 TABLET in 1 BOTTLE (76420-258-60)
76420-667-01 76420-667 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20240208 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 100 TABLET in 1 BOTTLE (76420-667-01)
76420-667-30 76420-667 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20240208 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 30 TABLET in 1 BOTTLE (76420-667-30)
76420-667-60 76420-667 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20240208 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 60 TABLET in 1 BOTTLE (76420-667-60)
76420-667-90 76420-667 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20240208 N/A ANDA ANDA040489 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 90 TABLET in 1 BOTTLE (76420-667-90)
82804-121-30 82804-121 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20240723 N/A ANDA ANDA040489 Proficient Rx LP METHOCARBAMOL 500 mg/1 30 TABLET in 1 BOTTLE (82804-121-30)
82804-121-90 82804-121 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20240711 N/A ANDA ANDA040489 Proficient Rx LP METHOCARBAMOL 500 mg/1 90 TABLET in 1 BOTTLE (82804-121-90)
69584-611-50 69584-611 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Oxford Pharmaceuticals, LLC METHOCARBAMOL 500 mg/1 500 TABLET in 1 BOTTLE (69584-611-50)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase