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
51655-205-20	51655-205	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20230108	N/A	ANDA	ANDA209312	Northwind Health Company, LLC	METHOCARBAMOL	750 mg/1	20 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-205-20)
51655-205-52	51655-205	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20230413	N/A	ANDA	ANDA209312	Northwind Health Company, LLC	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-205-52)
70010-770-01	70010-770	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20200201	N/A	ANDA	ANDA209312	Granules Pharmaceuticals Inc.	METHOCARBAMOL	750 mg/1	100 TABLET, COATED in 1 BOTTLE (70010-770-01)
70010-770-05	70010-770	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20200201	N/A	ANDA	ANDA209312	Granules Pharmaceuticals Inc.	METHOCARBAMOL	750 mg/1	500 TABLET, COATED in 1 BOTTLE (70010-770-05)
68788-8172-9	68788-8172	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20220425	N/A	ANDA	ANDA209312	Preferred Pharmaceuticals Inc.	METHOCARBAMOL	750 mg/1	90 TABLET, COATED in 1 BOTTLE (68788-8172-9)
51655-195-51	51655-195	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20221216	N/A	ANDA	ANDA209312	Northwind Health Company, 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 Health Company, LLC	METHOCARBAMOL	500 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-52)
51655-195-84	51655-195	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20221116	N/A	ANDA	ANDA209312	Northwind Health Company, LLC	METHOCARBAMOL	500 mg/1	14 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-84)
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)