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
76420-258-90	76420-258	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20190815	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	90 TABLET in 1 BOTTLE (76420-258-90)
76420-258-60	76420-258	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20190815	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	60 TABLET in 1 BOTTLE (76420-258-60)
55700-990-30	55700-990	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20221215	20260430	ANDA	ANDA040489	Quality Care Products, LLC	METHOCARBAMOL	500 mg/1	30 TABLET in 1 BOTTLE (55700-990-30)
76420-258-30	76420-258	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20190815	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	30 TABLET in 1 BOTTLE (76420-258-30)
76420-258-10	76420-258	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20190815	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	100 TABLET in 1 BOTTLE (76420-258-10)
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)
45865-242-30	45865-242	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20240205	N/A	ANDA	ANDA040489	Medsource Pharmaceuticals	METHOCARBAMOL	500 mg/1	30 TABLET in 1 BOTTLE (45865-242-30)
45865-242-60	45865-242	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20230208	N/A	ANDA	ANDA040489	Medsource Pharmaceuticals	METHOCARBAMOL	500 mg/1	60 TABLET in 1 BOTTLE (45865-242-60)
76420-626-30	76420-626	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231017	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET in 1 BOTTLE (76420-626-30)
76420-626-60	76420-626	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231017	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	60 TABLET in 1 BOTTLE (76420-626-60)
76420-626-90	76420-626	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231017	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	90 TABLET in 1 BOTTLE (76420-626-90)
76420-626-01	76420-626	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231017	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	100 TABLET in 1 BOTTLE (76420-626-01)
76420-638-01	76420-638	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231017	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	100 TABLET in 1 BOTTLE (76420-638-01)
76420-667-01	76420-667	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240208	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	100 TABLET in 1 BOTTLE (76420-667-01)
76420-667-30	76420-667	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240208	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET in 1 BOTTLE (76420-667-30)
76420-667-60	76420-667	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240208	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	60 TABLET in 1 BOTTLE (76420-667-60)
76420-667-90	76420-667	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240208	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	90 TABLET in 1 BOTTLE (76420-667-90)
76420-638-30	76420-638	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231017	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	30 TABLET in 1 BOTTLE (76420-638-30)
76420-638-60	76420-638	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231017	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	60 TABLET in 1 BOTTLE (76420-638-60)
76420-638-90	76420-638	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231017	N/A	ANDA	ANDA040489	Asclemed USA, Inc.	METHOCARBAMOL	750 mg/1	90 TABLET in 1 BOTTLE (76420-638-90)