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
71610-832-92 71610-832 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20240510 N/A ANDA ANDA090200 Aphena Pharma Solutions - Tennessee, LLC METHOCARBAMOL 500 mg/1 270 TABLET in 1 BOTTLE (71610-832-92)
63187-087-00 63187-087 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 500 mg/1 100 TABLET in 1 BOTTLE (63187-087-00)
63187-087-20 63187-087 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 500 mg/1 20 TABLET in 1 BOTTLE (63187-087-20)
63187-087-30 63187-087 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 500 mg/1 30 TABLET in 1 BOTTLE (63187-087-30)
51655-575-20 51655-575 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20200824 N/A ANDA ANDA090200 Northwind Health Company, LLC METHOCARBAMOL 750 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (51655-575-20)
51655-575-52 51655-575 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20220330 N/A ANDA ANDA090200 Northwind Health Company, LLC METHOCARBAMOL 750 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (51655-575-52)
63187-019-00 63187-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 750 mg/1 100 TABLET in 1 BOTTLE (63187-019-00)
63187-019-20 63187-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 750 mg/1 20 TABLET in 1 BOTTLE (63187-019-20)
63187-019-30 63187-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 750 mg/1 30 TABLET in 1 BOTTLE (63187-019-30)
63187-019-40 63187-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 750 mg/1 40 TABLET in 1 BOTTLE (63187-019-40)
63187-019-45 63187-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20170901 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 750 mg/1 45 TABLET in 1 BOTTLE (63187-019-45)
63187-019-60 63187-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 750 mg/1 60 TABLET in 1 BOTTLE (63187-019-60)
63187-019-90 63187-019 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 750 mg/1 90 TABLET in 1 BOTTLE (63187-019-90)
63187-087-40 63187-087 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 500 mg/1 40 TABLET in 1 BOTTLE (63187-087-40)
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)
50090-0182-1 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)
50090-0182-3 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)
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)
72865-234-01 72865-234 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20240202 N/A ANDA ANDA090200 XLCare Pharmaceuticals Inc. METHOCARBAMOL 750 mg/1 100 TABLET in 1 BOTTLE (72865-234-01)
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