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 58 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
71335-2794-9 71335-2794 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 500 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71335-2794-9)
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)
71335-2795-3 71335-2795 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 40 TABLET, FILM COATED in 1 BOTTLE (71335-2795-3)
71335-2795-4 71335-2795 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-2795-4)
71335-2795-5 71335-2795 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2795-5)
71335-2795-6 71335-2795 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2795-6)
71335-2795-7 71335-2795 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 112 TABLET, FILM COATED in 1 BOTTLE (71335-2795-7)
71335-2795-8 71335-2795 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (71335-2795-8)
71335-2795-9 71335-2795 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA213967 Bryant Ranch Prepack METHOCARBAMOL 750 mg/1 84 TABLET, FILM COATED in 1 BOTTLE (71335-2795-9)
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)
87063-040-20 87063-040 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251124 N/A ANDA ANDA213967 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (87063-040-20)
87063-040-10 87063-040 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251124 N/A ANDA ANDA213967 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (87063-040-10)
87063-040-01 87063-040 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20251124 N/A ANDA ANDA213967 Asclemed USA, Inc. METHOCARBAMOL 500 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (87063-040-01)
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)
68071-3859-9 68071-3859 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol TABLET, FILM COATED ORAL 20250114 N/A ANDA ANDA213967 NuCare Pharmaceuticals,Inc. METHOCARBAMOL 750 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-3859-9)
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)
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