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"
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
72789-022-82 72789-022 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20191024 N/A ANDA ANDA208507 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 750 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-82)
72789-022-90 72789-022 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20230912 N/A ANDA ANDA208507 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 750 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-90)
72789-022-93 72789-022 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20230912 N/A ANDA ANDA208507 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 750 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-93)
72789-022-98 72789-022 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20230912 N/A ANDA ANDA208507 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 750 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-98)
72789-041-20 72789-041 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20200213 N/A ANDA ANDA208507 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 750 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-20)
72789-041-30 72789-041 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20200116 N/A ANDA ANDA208507 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-30)
72789-041-40 72789-041 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20200106 N/A ANDA ANDA208507 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 750 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-40)
72789-041-60 72789-041 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20191219 N/A ANDA ANDA208507 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 750 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-60)
72789-110-40 72789-110 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20200908 N/A ANDA ANDA208507 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 500 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-110-40)
50090-3578-1 50090-3578 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180913 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-3578-1)
50090-3578-3 50090-3578 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3578-3)
50090-3578-4 50090-3578 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20190411 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-3578-4)
50090-4793-0 50090-4793 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20191212 N/A ANDA ANDA208507 A-S Medication Solutions METHOCARBAMOL 500 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (50090-4793-0)
71335-0828-0 71335-0828 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-0828-0)
71335-0828-1 71335-0828 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-0828-1)
71335-0828-2 71335-0828 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0828-2)
71335-0828-3 71335-0828 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-0828-3)
71335-0828-4 71335-0828 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0828-4)
71335-0828-5 71335-0828 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0828-5)
71335-0828-6 71335-0828 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20180115 N/A ANDA ANDA208507 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0828-6)
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