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=ANDA209312"
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
68071-4520-2 68071-4520 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180808 N/A ANDA ANDA209312 NuCare Pharmaceuticals,Inc. METHOCARBAMOL 500 mg/1 20 TABLET, COATED in 1 BOTTLE (68071-4520-2)
68071-4520-3 68071-4520 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180808 N/A ANDA ANDA209312 NuCare Pharmaceuticals,Inc. METHOCARBAMOL 500 mg/1 30 TABLET, COATED in 1 BOTTLE (68071-4520-3)
68071-4520-6 68071-4520 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250114 N/A ANDA ANDA209312 NuCare Pharmaceuticals,Inc. METHOCARBAMOL 500 mg/1 60 TABLET, COATED in 1 BOTTLE (68071-4520-6)
68071-4520-9 68071-4520 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20260130 N/A ANDA ANDA209312 NuCare Pharmaceuticals,Inc. METHOCARBAMOL 500 mg/1 90 TABLET, COATED in 1 BOTTLE (68071-4520-9)
70010-754-01 70010-754 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20200201 N/A ANDA ANDA209312 Granules Pharmaceuticals Inc. METHOCARBAMOL 500 mg/1 100 TABLET, COATED in 1 BOTTLE (70010-754-01)
70010-754-05 70010-754 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20200201 N/A ANDA ANDA209312 Granules Pharmaceuticals Inc. METHOCARBAMOL 500 mg/1 500 TABLET, COATED in 1 BOTTLE (70010-754-05)
68788-8172-3 68788-8172 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20220425 N/A ANDA ANDA209312 Preferred Pharmaceuticals Inc. METHOCARBAMOL 750 mg/1 30 TABLET, COATED in 1 BOTTLE (68788-8172-3)
68788-8172-6 68788-8172 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20220425 N/A ANDA ANDA209312 Preferred Pharmaceuticals Inc. METHOCARBAMOL 750 mg/1 60 TABLET, COATED in 1 BOTTLE (68788-8172-6)
68788-8172-9 68788-8172 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20220425 N/A ANDA ANDA209312 Preferred Pharmaceuticals Inc. METHOCARBAMOL 750 mg/1 90 TABLET, COATED in 1 BOTTLE (68788-8172-9)
62207-770-41 62207-770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180515 N/A ANDA ANDA209312 Granules India Ltd METHOCARBAMOL 750 mg/1 24 TABLET, COATED in 1 BOTTLE (62207-770-41)
80425-0579-1 80425-0579 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250325 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 30 TABLET, COATED in 1 BOTTLE (80425-0579-1)
43063-903-18 43063-903 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20220502 N/A ANDA ANDA209312 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 500 mg/1 18 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-18)
43063-903-20 43063-903 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181108 N/A ANDA ANDA209312 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 500 mg/1 20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-20)
80425-0579-2 80425-0579 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250325 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 60 TABLET, COATED in 1 BOTTLE (80425-0579-2)
80425-0579-3 80425-0579 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250325 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 90 TABLET, COATED in 1 BOTTLE (80425-0579-3)
80425-0579-4 80425-0579 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250325 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 120 TABLET, COATED in 1 BOTTLE (80425-0579-4)
80425-0579-5 80425-0579 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250325 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 180 TABLET, COATED in 1 BOTTLE (80425-0579-5)
80425-0579-6 80425-0579 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250325 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 12 TABLET, COATED in 1 BOTTLE (80425-0579-6)
62207-754-41 62207-754 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180515 N/A ANDA ANDA209312 Granules India Ltd METHOCARBAMOL 500 mg/1 24 TABLET, COATED in 1 BOTTLE (62207-754-41)
62207-754-43 62207-754 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180515 N/A ANDA ANDA209312 Granules India Ltd METHOCARBAMOL 500 mg/1 100 TABLET, COATED in 1 BOTTLE (62207-754-43)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase