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
50090-3570-0 50090-3570 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180702 N/A ANDA ANDA209312 A-S Medication Solutions METHOCARBAMOL 500 mg/1 10 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3570-0)
50090-3570-4 50090-3570 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180702 N/A ANDA ANDA209312 A-S Medication Solutions METHOCARBAMOL 500 mg/1 90 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3570-4)
50090-3587-0 50090-3587 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20180926 N/A ANDA ANDA209312 A-S Medication Solutions METHOCARBAMOL 750 mg/1 90 TABLET, COATED in 1 BOTTLE (50090-3587-0)
50090-3756-0 50090-3756 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181031 N/A ANDA ANDA209312 A-S Medication Solutions METHOCARBAMOL 500 mg/1 40 TABLET, COATED in 1 BOTTLE (50090-3756-0)
70518-4501-0 70518-4501 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20251013 N/A ANDA ANDA209312 REMEDYREPACK INC. METHOCARBAMOL 750 mg/1 40 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-4501-0)
70934-756-30 70934-756 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20220503 20260331 ANDA ANDA209312 Denton Pharma, Inc. dba Northwind Pharmaceuticals METHOCARBAMOL 750 mg/1 30 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-756-30)
51655-195-51 51655-195 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20221216 N/A ANDA ANDA209312 Northwind Health Company, LLC METHOCARBAMOL 500 mg/1 40 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-51)
51655-195-52 51655-195 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20221216 N/A ANDA ANDA209312 Northwind Health Company, LLC METHOCARBAMOL 500 mg/1 30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-52)
51655-195-84 51655-195 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20221116 N/A ANDA ANDA209312 Northwind Health Company, LLC METHOCARBAMOL 500 mg/1 14 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-84)
51655-205-20 51655-205 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20230108 N/A ANDA ANDA209312 Northwind Health Company, LLC METHOCARBAMOL 750 mg/1 20 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-205-20)
51655-205-52 51655-205 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20230413 N/A ANDA ANDA209312 Northwind Health Company, LLC METHOCARBAMOL 750 mg/1 30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-205-52)
67296-2197-1 67296-2197 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20200201 N/A ANDA ANDA209312 Redpharm Drug METHOCARBAMOL 500 mg/1 15 TABLET, COATED in 1 BOTTLE (67296-2197-1)
67296-2197-3 67296-2197 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20200201 N/A ANDA ANDA209312 Redpharm Drug METHOCARBAMOL 500 mg/1 30 TABLET, COATED in 1 BOTTLE (67296-2197-3)
43063-903-18 43063-903 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20220502 N/A ANDA ANDA209312 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 500 mg/1 18 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-18)
43063-903-20 43063-903 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181108 N/A ANDA ANDA209312 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 500 mg/1 20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-20)
43063-903-24 43063-903 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20190225 N/A ANDA ANDA209312 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 500 mg/1 24 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-24)
43063-903-28 43063-903 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181108 N/A ANDA ANDA209312 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 500 mg/1 28 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-28)
43063-903-30 43063-903 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181114 N/A ANDA ANDA209312 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 500 mg/1 30 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-903-30)
43063-905-14 43063-905 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181108 N/A ANDA ANDA209312 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 750 mg/1 14 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-14)
43063-905-20 43063-905 HUMAN PRESCRIPTION DRUG Methocarbamol Methocarbamol Tablets TABLET, COATED ORAL 20181108 N/A ANDA ANDA209312 PD-Rx Pharmaceuticals, Inc. METHOCARBAMOL 750 mg/1 20 TABLET, COATED in 1 BOTTLE, PLASTIC (43063-905-20)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase