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
72789-499-20	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)
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)
72789-521-40	72789-521	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 750 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20260323	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-40)
72789-521-60	72789-521	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 750 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250918	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-60)
72789-521-82	72789-521	HUMAN PRESCRIPTION DRUG	Methocarbamol Tablets, USP, 750 mg	Methocarbamol	TABLET, FILM COATED	ORAL	20250815	N/A	ANDA	ANDA212623	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-521-82)