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
71335-2305-8 71335-2305 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20240403 N/A ANDA ANDA040489 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 21 TABLET in 1 BOTTLE (71335-2305-8)
71335-2305-9 71335-2305 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20240403 N/A ANDA ANDA040489 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 84 TABLET in 1 BOTTLE (71335-2305-9)
85509-1910-1 85509-1910 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20250711 N/A ANDA ANDA040489 PHOENIX RX LLC METHOCARBAMOL 500 mg/1 100 TABLET in 1 BOTTLE (85509-1910-1)
85509-1910-3 85509-1910 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20251111 N/A ANDA ANDA040489 PHOENIX RX LLC METHOCARBAMOL 500 mg/1 30 TABLET in 1 BOTTLE (85509-1910-3)
85509-1910-6 85509-1910 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20250714 N/A ANDA ANDA040489 PHOENIX RX LLC METHOCARBAMOL 500 mg/1 60 TABLET in 1 BOTTLE (85509-1910-6)
85509-1910-9 85509-1910 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20250714 N/A ANDA ANDA040489 PHOENIX RX LLC METHOCARBAMOL 500 mg/1 90 TABLET in 1 BOTTLE (85509-1910-9)
72162-1929-1 72162-1929 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Bryant Ranch Prepack METHOCARBAMOL 500 mg/1 100 TABLET in 1 BOTTLE (72162-1929-1)
72162-1929-5 72162-1929 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Bryant Ranch Prepack METHOCARBAMOL 500 mg/1 500 TABLET in 1 BOTTLE (72162-1929-5)
72162-1930-1 72162-1930 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 100 TABLET in 1 BOTTLE (72162-1930-1)
72162-1930-5 72162-1930 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20190815 N/A ANDA ANDA040489 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 500 TABLET in 1 BOTTLE (72162-1930-5)
15014-910-10 15014-910 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20250522 N/A ANDA ANDA040489 GENTEX PHARMA, LLC METHOCARBAMOL 500 mg/1 100 TABLET in 1 BOTTLE (15014-910-10)
50090-5006-0 50090-5006 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20200415 N/A ANDA ANDA040489 A-S Medication Solutions METHOCARBAMOL 750 mg/1 90 TABLET in 1 BOTTLE (50090-5006-0)
50090-5008-1 50090-5008 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20200415 N/A ANDA ANDA040489 A-S Medication Solutions METHOCARBAMOL 750 mg/1 40 TABLET in 1 BOTTLE (50090-5008-1)
50090-5008-2 50090-5008 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20200415 N/A ANDA ANDA040489 A-S Medication Solutions METHOCARBAMOL 750 mg/1 28 TABLET in 1 BOTTLE (50090-5008-2)
50090-5008-3 50090-5008 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20200415 N/A ANDA ANDA040489 A-S Medication Solutions METHOCARBAMOL 750 mg/1 30 TABLET in 1 BOTTLE (50090-5008-3)
50090-5008-4 50090-5008 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20200415 N/A ANDA ANDA040489 A-S Medication Solutions METHOCARBAMOL 750 mg/1 60 TABLET in 1 BOTTLE (50090-5008-4)
50090-5008-6 50090-5008 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20200415 N/A ANDA ANDA040489 A-S Medication Solutions METHOCARBAMOL 750 mg/1 100 TABLET in 1 BOTTLE (50090-5008-6)
50090-5008-7 50090-5008 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20200415 N/A ANDA ANDA040489 A-S Medication Solutions METHOCARBAMOL 750 mg/1 12 TABLET in 1 BOTTLE (50090-5008-7)
50090-5008-0 50090-5008 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20200415 N/A ANDA ANDA040489 A-S Medication Solutions METHOCARBAMOL 750 mg/1 20 TABLET in 1 BOTTLE (50090-5008-0)
50090-5846-0 50090-5846 HUMAN PRESCRIPTION DRUG Methocarbamol methocarbamol TABLET ORAL 20211105 N/A ANDA ANDA040489 A-S Medication Solutions METHOCARBAMOL 500 mg/1 10 TABLET in 1 BOTTLE (50090-5846-0)
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