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
71205-167-90	71205-167	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20181201	N/A	ANDA	ANDA209312	Proficient Rx LP	METHOCARBAMOL	500 mg/1	90 TABLET, COATED in 1 BOTTLE (71205-167-90)
71610-134-60	71610-134	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180827	N/A	ANDA	ANDA209312	Aphena Pharma Solutions - Tennessee, LLC	METHOCARBAMOL	750 mg/1	90 TABLET, COATED in 1 BOTTLE (71610-134-60)
71610-134-53	71610-134	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180827	N/A	ANDA	ANDA209312	Aphena Pharma Solutions - Tennessee, LLC	METHOCARBAMOL	750 mg/1	60 TABLET, COATED in 1 BOTTLE (71610-134-53)
85509-1770-9	85509-1770	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20251016	N/A	ANDA	ANDA209312	PHOENIX RX LLC	METHOCARBAMOL	750 mg/1	90 TABLET, COATED in 1 BOTTLE (85509-1770-9)
85509-1770-3	85509-1770	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20251016	N/A	ANDA	ANDA209312	PHOENIX RX LLC	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BOTTLE (85509-1770-3)
85509-1770-6	85509-1770	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20251016	N/A	ANDA	ANDA209312	PHOENIX RX LLC	METHOCARBAMOL	750 mg/1	60 TABLET, COATED in 1 BOTTLE (85509-1770-6)