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）

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
72789-110-40	72789-110	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200908	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-110-40)
67296-1825-3	67296-1825	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	RedPharm Drug, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67296-1825-3)
50090-3578-1	50090-3578	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180913	N/A	ANDA	ANDA208507	A-S Medication Solutions	METHOCARBAMOL	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (50090-3578-1)
50090-3578-3	50090-3578	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	A-S Medication Solutions	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3578-3)
50090-3578-4	50090-3578	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20190411	N/A	ANDA	ANDA208507	A-S Medication Solutions	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-3578-4)
76420-040-30	76420-040	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA208507	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (76420-040-30)
76420-040-60	76420-040	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200123	N/A	ANDA	ANDA208507	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (76420-040-60)
76385-124-01	76385-124	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	Bayshore Pharmaceuticals LLC	METHOCARBAMOL	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76385-124-01)
76385-124-50	76385-124	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	Bayshore Pharmaceuticals LLC	METHOCARBAMOL	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76385-124-50)
80425-0171-1	80425-0171	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	Advanced Rx Pharmacy of Tennessee, LLC	METHOCARBAMOL	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0171-1)
80425-0171-2	80425-0171	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	Advanced Rx Pharmacy of Tennessee, LLC	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0171-2)
80425-0171-3	80425-0171	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	Advanced Rx Pharmacy of Tennessee, LLC	METHOCARBAMOL	750 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0171-3)
72789-022-98	72789-022	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20230912	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-98)
71610-242-53	71610-242	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20190222	N/A	ANDA	ANDA208507	Aphena Pharma Solutions - Tennessee, LLC	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-242-53)
71610-242-70	71610-242	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20190222	N/A	ANDA	ANDA208507	Aphena Pharma Solutions - Tennessee, LLC	METHOCARBAMOL	750 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71610-242-70)
71610-242-80	71610-242	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20190222	N/A	ANDA	ANDA208507	Aphena Pharma Solutions - Tennessee, LLC	METHOCARBAMOL	750 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71610-242-80)
80425-0138-1	80425-0138	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	Advanced Rx Pharmacy of Tennessee, LLC	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0138-1)
80425-0138-2	80425-0138	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	Advanced Rx Pharmacy of Tennessee, LLC	METHOCARBAMOL	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0138-2)
71335-0828-5	71335-0828	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0828-5)
50090-4793-0	50090-4793	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191212	N/A	ANDA	ANDA208507	A-S Medication Solutions	METHOCARBAMOL	500 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (50090-4793-0)