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
80425-0578-2 80425-0578 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20260313 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 60 TABLET, COATED in 1 BOTTLE (80425-0578-2)
60760-770-28 60760-770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20220720 N/A ANDA ANDA209312 St. Mary's Medical Park Pharmacy METHOCARBAMOL 750 mg/1 28 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-770-28)
60760-770-30 60760-770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20260330 N/A ANDA ANDA209312 St. Mary's Medical Park Pharmacy METHOCARBAMOL 750 mg/1 30 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-770-30)
60760-770-40 60760-770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181115 N/A ANDA ANDA209312 St. Mary's Medical Park Pharmacy METHOCARBAMOL 750 mg/1 40 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-770-40)
60760-770-60 60760-770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20221221 N/A ANDA ANDA209312 St. Mary's Medical Park Pharmacy METHOCARBAMOL 750 mg/1 60 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-770-60)
60760-770-90 60760-770 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250213 N/A ANDA ANDA209312 St. Mary's Medical Park Pharmacy METHOCARBAMOL 750 mg/1 90 TABLET, COATED in 1 BOTTLE, PLASTIC (60760-770-90)
80425-0578-3 80425-0578 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20260313 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 90 TABLET, COATED in 1 BOTTLE (80425-0578-3)
80425-0578-4 80425-0578 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20260313 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 120 TABLET, COATED in 1 BOTTLE (80425-0578-4)
80425-0578-5 80425-0578 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20260313 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 180 TABLET, COATED in 1 BOTTLE (80425-0578-5)
80425-0578-6 80425-0578 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20260313 N/A ANDA ANDA209312 Advanced Rx of Tennessee, LLC METHOCARBAMOL 500 mg/1 12 TABLET, COATED in 1 BOTTLE (80425-0578-6)
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)
71205-167-90 71205-167 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181201 N/A ANDA ANDA209312 Proficient Rx LP METHOCARBAMOL 500 mg/1 90 TABLET, COATED in 1 BOTTLE (71205-167-90)
76420-893-01 76420-893 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 100 TABLET, COATED in 1 BOTTLE (76420-893-01)
76420-893-05 76420-893 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 500 TABLET, COATED in 1 BOTTLE (76420-893-05)
76420-893-12 76420-893 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 120 TABLET, COATED in 1 BOTTLE (76420-893-12)
76420-893-30 76420-893 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 30 TABLET, COATED in 1 BOTTLE (76420-893-30)
76420-893-60 76420-893 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 60 TABLET, COATED in 1 BOTTLE (76420-893-60)
76420-893-90 76420-893 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20250128 N/A ANDA ANDA209312 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 90 TABLET, COATED in 1 BOTTLE (76420-893-90)
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)
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