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=ANDA090200"
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
72865-233-05 72865-233 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20240202 N/A ANDA ANDA090200 XLCare Pharmaceuticals Inc. METHOCARBAMOL 500 mg/1 500 TABLET in 1 BOTTLE (72865-233-05)
72865-233-01 72865-233 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20240202 N/A ANDA ANDA090200 XLCare Pharmaceuticals Inc. METHOCARBAMOL 500 mg/1 100 TABLET in 1 BOTTLE (72865-233-01)
72865-234-05 72865-234 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20240202 N/A ANDA ANDA090200 XLCare Pharmaceuticals Inc. METHOCARBAMOL 750 mg/1 500 TABLET in 1 BOTTLE (72865-234-05)
61919-903-90 61919-903 HUMAN PRESCRIPTION DRUG METHOCARBAMOL METHOCARBAMOL TABLET ORAL 20190423 N/A ANDA ANDA090200 DirectRX METHOCARBAMOL 750 mg/1 90 TABLET in 1 BOTTLE (61919-903-90)
61919-903-72 61919-903 HUMAN PRESCRIPTION DRUG METHOCARBAMOL METHOCARBAMOL TABLET ORAL 20190829 N/A ANDA ANDA090200 Direct_Rx METHOCARBAMOL 750 mg/1 120 TABLET in 1 BOTTLE (61919-903-72)
61919-903-30 61919-903 HUMAN PRESCRIPTION DRUG METHOCARBAMOL METHOCARBAMOL TABLET ORAL 20190827 N/A ANDA ANDA090200 Direct_Rx METHOCARBAMOL 750 mg/1 30 TABLET in 1 BOTTLE (61919-903-30)
61919-903-40 61919-903 HUMAN PRESCRIPTION DRUG METHOCARBAMOL METHOCARBAMOL TABLET ORAL 20190829 N/A ANDA ANDA090200 Direct_Rx METHOCARBAMOL 750 mg/1 40 TABLET in 1 BOTTLE (61919-903-40)
61919-903-60 61919-903 HUMAN PRESCRIPTION DRUG METHOCARBAMOL METHOCARBAMOL TABLET ORAL 20190829 N/A ANDA ANDA090200 Direct_Rx METHOCARBAMOL 750 mg/1 60 TABLET in 1 BOTTLE (61919-903-60)
50090-0182-0 50090-0182 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20141128 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 40 TABLET in 1 BOTTLE (50090-0182-0)
50090-0182-4 50090-0182 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20141128 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 30 TABLET in 1 BOTTLE (50090-0182-4)
50090-0182-5 50090-0182 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20141128 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 14 TABLET in 1 BOTTLE (50090-0182-5)
50090-0182-8 50090-0182 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20200812 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 56 TABLET in 1 BOTTLE (50090-0182-8)
50090-0183-0 50090-0183 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20160621 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 10 TABLET in 1 BOTTLE (50090-0183-0)
50090-0183-2 50090-0183 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20141128 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 7 TABLET in 1 BOTTLE (50090-0183-2)
50090-0183-4 50090-0183 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20141128 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 90 TABLET in 1 BOTTLE (50090-0183-4)
50090-0184-0 50090-0184 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20141128 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 40 TABLET in 1 BOTTLE (50090-0184-0)
50090-0182-1 50090-0182 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20160621 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 20 TABLET in 1 BOTTLE (50090-0182-1)
50090-0182-2 50090-0182 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20200812 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 80 TABLET in 1 BOTTLE (50090-0182-2)
50090-0182-3 50090-0182 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20141128 N/A ANDA ANDA090200 A-S Medication Solutions METHOCARBAMOL 500 mg/1 60 TABLET in 1 BOTTLE (50090-0182-3)
67296-1049-3 67296-1049 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20130320 N/A ANDA ANDA090200 RedPharm Drug, Inc. METHOCARBAMOL 750 mg/1 30 TABLET in 1 BOTTLE (67296-1049-3)
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