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
72789-041-20	72789-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200213	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-20)
72789-041-30	72789-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200116	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-30)
72789-041-40	72789-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200106	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-40)
72789-041-60	72789-041	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191219	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-041-60)