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
59651-340-01	59651-340	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20230209	N/A	ANDA	ANDA213967	Aurobindo Pharma Limited	METHOCARBAMOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-340-01)
0615-8506-05	0615-8506	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20240701	N/A	ANDA	ANDA213967	NCS HealthCare of KY, LLC dba Vangard Labs	METHOCARBAMOL	500 mg/1	15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8506-05)
0615-8506-39	0615-8506	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20240411	N/A	ANDA	ANDA213967	NCS HealthCare of KY, LLC dba Vangard Labs	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8506-39)
0615-8507-39	0615-8507	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20240312	N/A	ANDA	ANDA213967	NCS HealthCare of KY, LLC dba Vangard Labs	METHOCARBAMOL	750 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8507-39)
59651-341-05	59651-341	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200812	N/A	ANDA	ANDA213967	Aurobindo Pharma Limited	METHOCARBAMOL	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (59651-341-05)
59651-341-01	59651-341	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20200812	N/A	ANDA	ANDA213967	Aurobindo Pharma Limited	METHOCARBAMOL	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (59651-341-01)
59651-340-05	59651-340	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20230209	N/A	ANDA	ANDA213967	Aurobindo Pharma Limited	METHOCARBAMOL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (59651-340-05)