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
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)
85766-060-01	85766-060	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250829	N/A	ANDA	ANDA213967	Sportpharm, Inc. dba Sportpharm	METHOCARBAMOL	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (85766-060-01)
85766-060-05	85766-060	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250829	N/A	ANDA	ANDA213967	Sportpharm, Inc. dba Sportpharm	METHOCARBAMOL	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (85766-060-05)
85766-060-28	85766-060	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250829	N/A	ANDA	ANDA213967	Sportpharm, Inc. dba Sportpharm	METHOCARBAMOL	750 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (85766-060-28)
85766-060-30	85766-060	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250829	N/A	ANDA	ANDA213967	Sportpharm, Inc. dba Sportpharm	METHOCARBAMOL	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (85766-060-30)
85766-060-42	85766-060	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250829	N/A	ANDA	ANDA213967	Sportpharm, Inc. dba Sportpharm	METHOCARBAMOL	750 mg/1	42 TABLET, FILM COATED in 1 BOTTLE (85766-060-42)
85766-060-60	85766-060	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250829	N/A	ANDA	ANDA213967	Sportpharm, Inc. dba Sportpharm	METHOCARBAMOL	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (85766-060-60)
85766-060-90	85766-060	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250829	N/A	ANDA	ANDA213967	Sportpharm, Inc. dba Sportpharm	METHOCARBAMOL	750 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (85766-060-90)
67296-2193-1	67296-2193	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20230209	N/A	ANDA	ANDA213967	Redpharm Drug	METHOCARBAMOL	500 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (67296-2193-1)
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)
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)
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)
59651-341-05	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)
68071-3859-2	68071-3859	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250604	N/A	ANDA	ANDA213967	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	750 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68071-3859-2)
68071-3859-3	68071-3859	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251224	N/A	ANDA	ANDA213967	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-3859-3)
68071-3859-9	68071-3859	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250114	N/A	ANDA	ANDA213967	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	750 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-3859-9)
68788-8867-3	68788-8867	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250423	N/A	ANDA	ANDA213967	Preferred Pharmaceuticals Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8867-3)
68788-8867-6	68788-8867	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20250423	N/A	ANDA	ANDA213967	Preferred Pharmaceuticals Inc.	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8867-6)