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
71335-2795-6	71335-2795	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2795-6)
71335-2795-7	71335-2795	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	112 TABLET, FILM COATED in 1 BOTTLE (71335-2795-7)
71335-2795-8	71335-2795	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-2795-8)
71335-2795-9	71335-2795	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	84 TABLET, FILM COATED in 1 BOTTLE (71335-2795-9)
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)
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)
71335-2794-0	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-2794-0)
71335-2794-1	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-2794-1)
71335-2794-2	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2794-2)
71335-2794-3	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-2794-3)
71335-2794-4	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2794-4)
71335-2794-5	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2794-5)
71335-2794-6	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-2794-6)
71335-2794-7	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2794-7)
71335-2794-8	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2794-8)
71335-2794-9	71335-2794	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, FILM COATED	ORAL	20251013	N/A	ANDA	ANDA213967	Bryant Ranch Prepack	METHOCARBAMOL	500 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-2794-9)