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
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)
63187-087-00 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)
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)
63187-087-60 63187-087 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 500 mg/1 60 TABLET in 1 BOTTLE (63187-087-60)
63187-087-90 63187-087 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20140401 N/A ANDA ANDA090200 Proficient Rx LP METHOCARBAMOL 500 mg/1 90 TABLET in 1 BOTTLE (63187-087-90)
66267-803-06 66267-803 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20200130 N/A ANDA ANDA090200 NuCare Pharmaceuticals,Inc. METHOCARBAMOL 750 mg/1 6 TABLET in 1 BOTTLE (66267-803-06)
71335-0251-0 71335-0251 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20211227 N/A ANDA ANDA090200 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 14 TABLET in 1 BOTTLE (71335-0251-0)
71335-0251-1 71335-0251 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20190325 N/A ANDA ANDA090200 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 20 TABLET in 1 BOTTLE (71335-0251-1)
71335-0251-2 71335-0251 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20180312 N/A ANDA ANDA090200 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 30 TABLET in 1 BOTTLE (71335-0251-2)
71335-0251-3 71335-0251 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20180313 N/A ANDA ANDA090200 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 40 TABLET in 1 BOTTLE (71335-0251-3)
71335-0251-4 71335-0251 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20180216 N/A ANDA ANDA090200 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 120 TABLET in 1 BOTTLE (71335-0251-4)
71335-0251-5 71335-0251 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20180307 N/A ANDA ANDA090200 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 60 TABLET in 1 BOTTLE (71335-0251-5)
71335-0251-6 71335-0251 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20180308 N/A ANDA ANDA090200 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 90 TABLET in 1 BOTTLE (71335-0251-6)
71335-0251-7 71335-0251 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20211227 N/A ANDA ANDA090200 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 112 TABLET in 1 BOTTLE (71335-0251-7)
71335-0251-8 71335-0251 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20211227 N/A ANDA ANDA090200 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 21 TABLET in 1 BOTTLE (71335-0251-8)
71335-0251-9 71335-0251 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET ORAL 20211227 N/A ANDA ANDA090200 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 84 TABLET in 1 BOTTLE (71335-0251-9)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase