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
51655-574-84	51655-574	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20200916	N/A	ANDA	ANDA090200	Northwind Pharmaceuticals, LLC	METHOCARBAMOL	500 mg/1	14 TABLET in 1 BOTTLE, PLASTIC (51655-574-84)
51655-575-20	51655-575	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20200824	N/A	ANDA	ANDA090200	Northwind Pharmaceuticals	METHOCARBAMOL	750 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (51655-575-20)
51655-575-52	51655-575	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20220330	N/A	ANDA	ANDA090200	Northwind Pharmaceuticals	METHOCARBAMOL	750 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-575-52)
53002-3042-1	53002-3042	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20220701	N/A	ANDA	ANDA090200	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	10 TABLET in 1 BOTTLE (53002-3042-1)
53002-3042-2	53002-3042	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20220701	N/A	ANDA	ANDA090200	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	20 TABLET in 1 BOTTLE (53002-3042-2)
53002-3042-3	53002-3042	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20220701	N/A	ANDA	ANDA090200	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET in 1 BOTTLE (53002-3042-3)
53002-3042-6	53002-3042	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20220701	N/A	ANDA	ANDA090200	RPK Pharmaceuticals, Inc.	METHOCARBAMOL	500 mg/1	60 TABLET in 1 BOTTLE (53002-3042-6)
35356-887-90	35356-887	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20130320	N/A	ANDA	ANDA090200	Quality Care Products LLC	METHOCARBAMOL	500 mg/1	90 TABLET in 1 BOTTLE (35356-887-90)
35356-887-30	35356-887	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20211126	N/A	ANDA	ANDA090200	Quality Care Products LLC	METHOCARBAMOL	500 mg/1	30 TABLET in 1 BOTTLE (35356-887-30)
35356-887-60	35356-887	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20130320	N/A	ANDA	ANDA090200	Quality Care Products LLC	METHOCARBAMOL	500 mg/1	60 TABLET in 1 BOTTLE (35356-887-60)
55700-218-30	55700-218	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20211126	N/A	ANDA	ANDA090200	Quality Care Products LLC	METHOCARBAMOL	750 mg/1	30 TABLET in 1 BOTTLE (55700-218-30)
55700-218-60	55700-218	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20211126	N/A	ANDA	ANDA090200	Quality Care Products LLC	METHOCARBAMOL	750 mg/1	60 TABLET in 1 BOTTLE (55700-218-60)
55700-218-90	55700-218	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20211126	N/A	ANDA	ANDA090200	Quality Care Products LLC	METHOCARBAMOL	750 mg/1	90 TABLET in 1 BOTTLE (55700-218-90)
63187-019-00	63187-019	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20140401	N/A	ANDA	ANDA090200	Proficient Rx LP	METHOCARBAMOL	750 mg/1	100 TABLET in 1 BOTTLE (63187-019-00)
63187-019-20	63187-019	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20140401	N/A	ANDA	ANDA090200	Proficient Rx LP	METHOCARBAMOL	750 mg/1	20 TABLET in 1 BOTTLE (63187-019-20)
63187-019-30	63187-019	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20140401	N/A	ANDA	ANDA090200	Proficient Rx LP	METHOCARBAMOL	750 mg/1	30 TABLET in 1 BOTTLE (63187-019-30)
63187-019-40	63187-019	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20140401	N/A	ANDA	ANDA090200	Proficient Rx LP	METHOCARBAMOL	750 mg/1	40 TABLET in 1 BOTTLE (63187-019-40)
63187-019-45	63187-019	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20170901	N/A	ANDA	ANDA090200	Proficient Rx LP	METHOCARBAMOL	750 mg/1	45 TABLET in 1 BOTTLE (63187-019-45)
63187-019-60	63187-019	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20140401	N/A	ANDA	ANDA090200	Proficient Rx LP	METHOCARBAMOL	750 mg/1	60 TABLET in 1 BOTTLE (63187-019-60)
63187-019-90	63187-019	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20140401	N/A	ANDA	ANDA090200	Proficient Rx LP	METHOCARBAMOL	750 mg/1	90 TABLET in 1 BOTTLE (63187-019-90)