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
60760-725-28	60760-725	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20230728	N/A	ANDA	ANDA040489	ST. MARY'S MEDICAL PARK PHARMACY	METHOCARBAMOL	750 mg/1	28 TABLET in 1 BOTTLE, PLASTIC (60760-725-28)
60760-725-40	60760-725	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20190815	N/A	ANDA	ANDA040489	ST. MARY'S MEDICAL PARK PHARMACY	METHOCARBAMOL	750 mg/1	40 TABLET in 1 BOTTLE, PLASTIC (60760-725-40)
60760-725-90	60760-725	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20230707	N/A	ANDA	ANDA040489	ST. MARY'S MEDICAL PARK PHARMACY	METHOCARBAMOL	750 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (60760-725-90)
69306-500-01	69306-500	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20250904	N/A	ANDA	ANDA040489	Doc Rx	METHOCARBAMOL	500 mg/1	100 TABLET in 1 BOTTLE (69306-500-01)
69306-500-60	69306-500	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20250904	N/A	ANDA	ANDA040489	Doc Rx	METHOCARBAMOL	500 mg/1	60 TABLET in 1 BOTTLE (69306-500-60)
69306-500-90	69306-500	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20250904	N/A	ANDA	ANDA040489	Doc Rx	METHOCARBAMOL	500 mg/1	90 TABLET in 1 BOTTLE (69306-500-90)
69306-510-01	69306-510	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20260319	N/A	ANDA	ANDA040489	Doc Rx	METHOCARBAMOL	500 mg/1	100 TABLET in 1 BOTTLE (69306-510-01)
69306-510-03	69306-510	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20260319	N/A	ANDA	ANDA040489	Doc Rx	METHOCARBAMOL	500 mg/1	30 TABLET in 1 BOTTLE (69306-510-03)
69306-510-06	69306-510	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20260319	N/A	ANDA	ANDA040489	Doc Rx	METHOCARBAMOL	500 mg/1	60 TABLET in 1 BOTTLE (69306-510-06)
69306-510-09	69306-510	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20260319	N/A	ANDA	ANDA040489	Doc Rx	METHOCARBAMOL	500 mg/1	90 TABLET in 1 BOTTLE (69306-510-09)
68071-3636-6	68071-3636	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240701	N/A	ANDA	ANDA040489	NuCare Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	6 TABLET in 1 BOTTLE (68071-3636-6)
55700-890-90	55700-890	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20210210	20260831	ANDA	ANDA040489	Quality Care Products, LLC	METHOCARBAMOL	500 mg/1	90 TABLET in 1 BOTTLE (55700-890-90)
71335-2305-0	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240403	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	14 TABLET in 1 BOTTLE (71335-2305-0)
71335-2305-1	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240403	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	20 TABLET in 1 BOTTLE (71335-2305-1)
71335-2305-2	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231215	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	30 TABLET in 1 BOTTLE (71335-2305-2)
71335-2305-3	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240403	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	40 TABLET in 1 BOTTLE (71335-2305-3)
71335-2305-4	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231127	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	120 TABLET in 1 BOTTLE (71335-2305-4)
71335-2305-5	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231228	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	60 TABLET in 1 BOTTLE (71335-2305-5)
71335-2305-6	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231116	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	90 TABLET in 1 BOTTLE (71335-2305-6)
71335-2305-7	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240403	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	112 TABLET in 1 BOTTLE (71335-2305-7)