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
72789-012-18	72789-012	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191219	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	18 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-18)
72789-012-20	72789-012	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20190920	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-20)
72789-012-24	72789-012	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20210505	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-24)
72789-012-30	72789-012	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20210810	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-30)
72789-012-40	72789-012	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200616	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-012-40)
72789-021-01	72789-021	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191024	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-01)
72789-021-60	72789-021	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20230912	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-60)
72789-021-82	72789-021	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191024	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-82)
72789-021-90	72789-021	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20230912	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-90)
72789-021-93	72789-021	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191024	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-93)
72789-021-94	72789-021	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191024	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-94)
72789-021-99	72789-021	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20191024	N/A	ANDA	ANDA208507	PD-Rx Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	240 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-021-99)
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)
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)
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)