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=ANDA208507"
符合检索条件的记录共 94 条，共 5 页，当前第 3 页 ，可点击列名称排序
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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
67296-1662-7 67296-1662 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA208507 RedPharm Drug, Inc. METHOCARBAMOL 750 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (67296-1662-7)
45865-987-60 45865-987 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20191211 N/A ANDA ANDA208507 medsource pharmaceuticals METHOCARBAMOL 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (45865-987-60)
80425-0138-1 80425-0138 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Advanced Rx Pharmacy of Tennessee, LLC METHOCARBAMOL 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0138-1)
80425-0138-2 80425-0138 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Advanced Rx Pharmacy of Tennessee, LLC METHOCARBAMOL 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0138-2)
67296-1825-3 67296-1825 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 RedPharm Drug, Inc. METHOCARBAMOL 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67296-1825-3)
80425-0171-1 80425-0171 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Advanced Rx Pharmacy of Tennessee, LLC METHOCARBAMOL 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0171-1)
80425-0171-2 80425-0171 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Advanced Rx Pharmacy of Tennessee, LLC METHOCARBAMOL 750 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0171-2)
80425-0171-3 80425-0171 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Advanced Rx Pharmacy of Tennessee, LLC METHOCARBAMOL 750 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0171-3)
76385-123-01 76385-123 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bayshore Pharmaceuticals LLC METHOCARBAMOL 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76385-123-01)
76385-123-50 76385-123 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bayshore Pharmaceuticals LLC METHOCARBAMOL 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76385-123-50)
50090-4162-0 50090-4162 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20190226 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 750 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-4162-0)
50090-4164-0 50090-4164 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20190226 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 750 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-4164-0)
50090-4164-1 50090-4164 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20190612 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 750 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (50090-4164-1)
50090-4164-2 50090-4164 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20190612 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 750 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (50090-4164-2)
50090-4164-3 50090-4164 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20190612 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-4164-3)
50090-4164-4 50090-4164 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20190612 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 750 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-4164-4)
50090-4164-6 50090-4164 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20190612 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 750 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-4164-6)
50090-4164-7 50090-4164 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20190612 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 750 mg/1 12 TABLET, FILM COATED in 1 BOTTLE (50090-4164-7)
76385-124-01 76385-124 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bayshore Pharmaceuticals LLC METHOCARBAMOL 750 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76385-124-01)
76385-124-50 76385-124 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bayshore Pharmaceuticals LLC METHOCARBAMOL 750 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76385-124-50)
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