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
72162-2487-1	72162-2487	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250505	N/A	ANDA	ANDA212623	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-2487-1)
72162-2487-5	72162-2487	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250505	N/A	ANDA	ANDA212623	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72162-2487-5)
72789-481-01	72789-481	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250610	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-01)
72789-481-30	72789-481	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250903	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-30)
72789-481-60	72789-481	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250610	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-60)
72789-481-82	72789-481	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250610	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-82)
72789-481-90	72789-481	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250610	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-90)
72789-481-93	72789-481	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250610	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-93)
72789-481-95	72789-481	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250610	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-481-95)
72162-2488-1	72162-2488	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 750 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250505	N/A	ANDA	ANDA212623	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (72162-2488-1)
72162-2488-5	72162-2488	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 750 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250505	N/A	ANDA	ANDA212623	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (72162-2488-5)
72789-499-18	72789-499	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250416	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	18 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-499-18)
72789-499-20	72789-499	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250428	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-499-20)
72789-499-28	72789-499	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250708	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-499-28)
10135-722-01	10135-722	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20211209	N/A	ANDA	ANDA212623	Marlex Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (10135-722-01)
10135-722-05	10135-722	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20211209	N/A	ANDA	ANDA212623	Marlex Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (10135-722-05)
63561-0173-1	63561-0173	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250610	N/A	ANDA	ANDA212623	Granulation Technology, Inc.	METHOCARBAMOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (63561-0173-1)
63561-0173-5	63561-0173	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 500 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250610	N/A	ANDA	ANDA212623	Granulation Technology, Inc.	METHOCARBAMOL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63561-0173-5)
72789-521-20	72789-521	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 750 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250829	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-20)
72789-521-30	72789-521	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 750 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20251024	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-30)