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=ANDA213967"
符合检索条件的记录共 61 条，共 4 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
67296-2193-1 67296-2193 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20230209 N/A ANDA ANDA213967 Redpharm Drug METHOCARBAMOL 500 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (67296-2193-1)
67296-2193-2 67296-2193 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20230209 N/A ANDA ANDA213967 Redpharm Drug METHOCARBAMOL 500 mg/1 24 TABLET, FILM COATED in 1 BOTTLE (67296-2193-2)
67296-2193-4 67296-2193 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20230209 N/A ANDA ANDA213967 Redpharm Drug METHOCARBAMOL 500 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (67296-2193-4)
59651-340-01 59651-340 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20230209 N/A ANDA ANDA213967 Aurobindo Pharma Limited METHOCARBAMOL 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (59651-340-01)
59651-340-05 59651-340 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20230209 N/A ANDA ANDA213967 Aurobindo Pharma Limited METHOCARBAMOL 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (59651-340-05)
87063-041-01 87063-041 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251124 N/A ANDA ANDA213967 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (87063-041-01)
87063-041-10 87063-041 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251124 N/A ANDA ANDA213967 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (87063-041-10)
87063-041-20 87063-041 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251124 N/A ANDA ANDA213967 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (87063-041-20)
87063-041-30 87063-041 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251124 N/A ANDA ANDA213967 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (87063-041-30)
87063-041-60 87063-041 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251124 N/A ANDA ANDA213967 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (87063-041-60)
59651-341-01 59651-341 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20200812 N/A ANDA ANDA213967 Aurobindo Pharma Limited METHOCARBAMOL 750 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (59651-341-01)
59651-341-05 59651-341 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20200812 N/A ANDA ANDA213967 Aurobindo Pharma Limited METHOCARBAMOL 750 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (59651-341-05)
68788-8867-3 68788-8867 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20250423 N/A ANDA ANDA213967 Preferred Pharmaceuticals Inc. METHOCARBAMOL 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8867-3)
68788-8867-6 68788-8867 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20250423 N/A ANDA ANDA213967 Preferred Pharmaceuticals Inc. METHOCARBAMOL 500 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8867-6)
68788-8867-9 68788-8867 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20250423 N/A ANDA ANDA213967 Preferred Pharmaceuticals Inc. METHOCARBAMOL 500 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8867-9)
0615-8506-05 0615-8506 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20240701 N/A ANDA ANDA213967 NCS HealthCare of KY, LLC dba Vangard Labs METHOCARBAMOL 500 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8506-05)
0615-8506-39 0615-8506 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20240411 N/A ANDA ANDA213967 NCS HealthCare of KY, LLC dba Vangard Labs METHOCARBAMOL 500 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8506-39)
87063-041-90 87063-041 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251124 N/A ANDA ANDA213967 Asclemed USA, Inc. METHOCARBAMOL 750 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (87063-041-90)
68071-3859-2 68071-3859 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20250604 N/A ANDA ANDA213967 NuCare Pharmaceuticals,Inc. METHOCARBAMOL 750 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-3859-2)
68071-3859-3 68071-3859 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251224 N/A ANDA ANDA213967 NuCare Pharmaceuticals,Inc. METHOCARBAMOL 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-3859-3)
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