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
72162-2488-1	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)
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)
63561-0174-1	63561-0174	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 750 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250610	N/A	ANDA	ANDA212623	Granulation Technology, Inc.	METHOCARBAMOL	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (63561-0174-1)
63561-0174-5	63561-0174	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 750 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250610	N/A	ANDA	ANDA212623	Granulation Technology, Inc.	METHOCARBAMOL	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63561-0174-5)