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 56 条，共 3 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
0615-8507-39 0615-8507 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20240312 N/A ANDA ANDA213967 NCS HealthCare of KY, LLC dba Vangard Labs METHOCARBAMOL 750 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8507-39)
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)
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)
71335-2794-0 71335-2794 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 500 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-2794-0)
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)
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)
85509-1341-3 85509-1341 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20250729 N/A ANDA ANDA213967 PHOENIX RX LLC METHOCARBAMOL 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (85509-1341-3)
85509-1341-6 85509-1341 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20250729 N/A ANDA ANDA213967 PHOENIX RX LLC METHOCARBAMOL 750 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (85509-1341-6)
71335-2795-0 71335-2795 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-2795-0)
71335-2795-1 71335-2795 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2795-1)
71335-2795-2 71335-2795 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2795-2)
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