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
66267-146-30	66267-146	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20161010	N/A	ANDA	ANDA090200	NuCare Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	30 TABLET in 1 BOTTLE (66267-146-30)
66267-146-40	66267-146	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20161010	N/A	ANDA	ANDA090200	NuCare Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	40 TABLET in 1 BOTTLE (66267-146-40)
66267-146-60	66267-146	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20161010	N/A	ANDA	ANDA090200	NuCare Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	60 TABLET in 1 BOTTLE (66267-146-60)
66267-146-90	66267-146	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20161010	N/A	ANDA	ANDA090200	NuCare Pharmaceuticals, Inc.	METHOCARBAMOL	750 mg/1	90 TABLET in 1 BOTTLE (66267-146-90)
66267-803-06	66267-803	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20200130	N/A	ANDA	ANDA090200	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	750 mg/1	6 TABLET in 1 BOTTLE (66267-803-06)
72865-233-01	72865-233	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20240202	N/A	ANDA	ANDA090200	XLCare Pharmaceuticals Inc.	METHOCARBAMOL	500 mg/1	100 TABLET in 1 BOTTLE (72865-233-01)
72865-233-05	72865-233	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20240202	N/A	ANDA	ANDA090200	XLCare Pharmaceuticals Inc.	METHOCARBAMOL	500 mg/1	500 TABLET in 1 BOTTLE (72865-233-05)
72865-234-01	72865-234	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20240202	N/A	ANDA	ANDA090200	XLCare Pharmaceuticals Inc.	METHOCARBAMOL	750 mg/1	100 TABLET in 1 BOTTLE (72865-234-01)
72865-234-05	72865-234	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20240202	N/A	ANDA	ANDA090200	XLCare Pharmaceuticals Inc.	METHOCARBAMOL	750 mg/1	500 TABLET in 1 BOTTLE (72865-234-05)