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
68071-4505-1	68071-4505	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180724	N/A	ANDA	ANDA209312	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	750 mg/1	21 TABLET, COATED in 1 BOTTLE (68071-4505-1)
68071-4505-2	68071-4505	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180724	N/A	ANDA	ANDA209312	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	750 mg/1	20 TABLET, COATED in 1 BOTTLE (68071-4505-2)
68071-4505-3	68071-4505	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20220525	N/A	ANDA	ANDA209312	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BOTTLE (68071-4505-3)
68071-4505-6	68071-4505	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180724	N/A	ANDA	ANDA209312	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	750 mg/1	60 TABLET, COATED in 1 BOTTLE (68071-4505-6)
82982-038-40	82982-038	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20230208	20270531	ANDA	ANDA209312	Pharmasource Meds, LLC	METHOCARBAMOL	750 mg/1	40 TABLET, COATED in 1 BOTTLE (82982-038-40)
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)
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)
61919-616-20	61919-616	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20190418	N/A	ANDA	ANDA209312	DIRECT RX	METHOCARBAMOL	750 mg/1	20 TABLET, COATED in 1 BOTTLE (61919-616-20)
61919-616-30	61919-616	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20190418	N/A	ANDA	ANDA209312	DIRECT RX	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BOTTLE (61919-616-30)
61919-616-60	61919-616	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20190418	N/A	ANDA	ANDA209312	DIRECT RX	METHOCARBAMOL	750 mg/1	60 TABLET, COATED in 1 BOTTLE (61919-616-60)
50090-3556-0	50090-3556	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180702	N/A	ANDA	ANDA209312	A-S Medication Solutions	METHOCARBAMOL	750 mg/1	20 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-0)
50090-3556-1	50090-3556	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180702	N/A	ANDA	ANDA209312	A-S Medication Solutions	METHOCARBAMOL	750 mg/1	40 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-1)
50090-3556-2	50090-3556	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180702	N/A	ANDA	ANDA209312	A-S Medication Solutions	METHOCARBAMOL	750 mg/1	28 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-2)
50090-3556-3	50090-3556	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180827	N/A	ANDA	ANDA209312	A-S Medication Solutions	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BOTTLE (50090-3556-3)
50090-3556-4	50090-3556	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180702	N/A	ANDA	ANDA209312	A-S Medication Solutions	METHOCARBAMOL	750 mg/1	60 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-4)
50090-3556-6	50090-3556	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180702	N/A	ANDA	ANDA209312	A-S Medication Solutions	METHOCARBAMOL	750 mg/1	100 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-6)
50090-3556-7	50090-3556	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180702	N/A	ANDA	ANDA209312	A-S Medication Solutions	METHOCARBAMOL	750 mg/1	12 TABLET, COATED in 1 BOTTLE, PLASTIC (50090-3556-7)
51655-195-51	51655-195	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20221216	N/A	ANDA	ANDA209312	Northwind Pharmaceuticals, LLC	METHOCARBAMOL	500 mg/1	40 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-51)
51655-195-52	51655-195	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20221216	N/A	ANDA	ANDA209312	Northwind Pharmaceuticals, LLC	METHOCARBAMOL	500 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-52)