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"
符合检索条件的记录共 115 条，共 6 页，当前第 2 页 ，可点击列名称排序
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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
76420-894-05 76420-894 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 500 TABLET, COATED in 1 BOTTLE (76420-894-05)
76420-894-12 76420-894 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 120 TABLET, COATED in 1 BOTTLE (76420-894-12)
76420-894-30 76420-894 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 30 TABLET, COATED in 1 BOTTLE (76420-894-30)
76420-894-60 76420-894 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 60 TABLET, COATED in 1 BOTTLE (76420-894-60)
76420-894-90 76420-894 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 90 TABLET, COATED in 1 BOTTLE (76420-894-90)
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)
70010-770-01 70010-770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20200201 N/A ANDA ANDA209312 Granules Pharmaceuticals Inc. METHOCARBAMOL 750 mg/1 100 TABLET, COATED in 1 BOTTLE (70010-770-01)
70010-770-05 70010-770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20200201 N/A ANDA ANDA209312 Granules Pharmaceuticals Inc. METHOCARBAMOL 750 mg/1 500 TABLET, COATED in 1 BOTTLE (70010-770-05)
80425-0020-1 80425-0020 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20180702 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 750 mg/1 30 TABLET, COATED in 1 BOTTLE (80425-0020-1)
80425-0020-2 80425-0020 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20180702 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 750 mg/1 60 TABLET, COATED in 1 BOTTLE (80425-0020-2)
80425-0020-3 80425-0020 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20180702 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 750 mg/1 90 TABLET, COATED in 1 BOTTLE (80425-0020-3)
61919-616-20 61919-616 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20190418 N/A ANDA ANDA209312 DIRECT RX METHOCARBAMOL 750 mg/1 20 TABLET, COATED in 1 BOTTLE (61919-616-20)
61919-616-30 61919-616 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20190418 N/A ANDA ANDA209312 DIRECT RX METHOCARBAMOL 750 mg/1 30 TABLET, COATED in 1 BOTTLE (61919-616-30)
61919-616-60 61919-616 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, COATED ORAL 20190418 N/A ANDA ANDA209312 DIRECT RX METHOCARBAMOL 750 mg/1 60 TABLET, COATED in 1 BOTTLE (61919-616-60)
85509-1770-3 85509-1770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20251016 N/A ANDA ANDA209312 PHOENIX RX LLC METHOCARBAMOL 750 mg/1 30 TABLET, COATED in 1 BOTTLE (85509-1770-3)
85509-1770-6 85509-1770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20251016 N/A ANDA ANDA209312 PHOENIX RX LLC METHOCARBAMOL 750 mg/1 60 TABLET, COATED in 1 BOTTLE (85509-1770-6)
85509-1770-9 85509-1770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20251016 N/A ANDA ANDA209312 PHOENIX RX LLC METHOCARBAMOL 750 mg/1 90 TABLET, COATED in 1 BOTTLE (85509-1770-9)
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)
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