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
72789-022-01	72789-022	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191024	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-01)
72789-022-82	72789-022	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191024	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-82)
72789-022-90	72789-022	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20230912	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-90)
72789-022-93	72789-022	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20230912	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-022-93)
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)
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)
71610-174-53	71610-174	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20181022	N/A	ANDA	ANDA208507	Aphena Pharma Solutions - Tennessee, LLC	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71610-174-53)
71610-174-60	71610-174	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20181022	N/A	ANDA	ANDA208507	Aphena Pharma Solutions - Tennessee, LLC	METHOCARBAMOL	750 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71610-174-60)
71610-174-70	71610-174	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20181022	N/A	ANDA	ANDA208507	Aphena Pharma Solutions - Tennessee, LLC	METHOCARBAMOL	750 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71610-174-70)
71610-174-80	71610-174	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20181022	N/A	ANDA	ANDA208507	Aphena Pharma Solutions - Tennessee, LLC	METHOCARBAMOL	750 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71610-174-80)
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)