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
53002-3041-2	53002-3041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20220701	N/A	ANDA	ANDA208507	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (53002-3041-2)
53002-3041-3	53002-3041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20220701	N/A	ANDA	ANDA208507	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (53002-3041-3)
53002-3041-6	53002-3041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20220701	N/A	ANDA	ANDA208507	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (53002-3041-6)
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)
71335-0828-8	71335-0828	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-0828-8)
71335-0828-9	71335-0828	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20180115	N/A	ANDA	ANDA208507	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	84 TABLET, FILM COATED in 1 BOTTLE (71335-0828-9)
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)
71335-0970-5	71335-0970	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20181018	N/A	ANDA	ANDA208507	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-0970-5)
71335-0970-6	71335-0970	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20181018	N/A	ANDA	ANDA208507	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-0970-6)
71335-0970-7	71335-0970	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20181018	N/A	ANDA	ANDA208507	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0970-7)
71335-0970-8	71335-0970	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20181018	N/A	ANDA	ANDA208507	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0970-8)
71335-0970-9	71335-0970	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20181018	N/A	ANDA	ANDA208507	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-0970-9)