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
68788-8213-3	68788-8213	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20220908	N/A	ANDA	ANDA209312	Preferred Pharmaceuticals Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, COATED in 1 BOTTLE (68788-8213-3)
68788-8213-6	68788-8213	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20220908	N/A	ANDA	ANDA209312	Preferred Pharmaceuticals Inc.	METHOCARBAMOL	500 mg/1	60 TABLET, COATED in 1 BOTTLE (68788-8213-6)
68788-8213-9	68788-8213	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20220908	N/A	ANDA	ANDA209312	Preferred Pharmaceuticals Inc.	METHOCARBAMOL	500 mg/1	90 TABLET, COATED in 1 BOTTLE (68788-8213-9)
68071-4520-2	68071-4520	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180808	N/A	ANDA	ANDA209312	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	500 mg/1	20 TABLET, COATED in 1 BOTTLE (68071-4520-2)
68071-4520-3	68071-4520	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180808	N/A	ANDA	ANDA209312	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, COATED in 1 BOTTLE (68071-4520-3)
68071-4520-6	68071-4520	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20250114	N/A	ANDA	ANDA209312	NuCare Pharmaceuticals,Inc.	METHOCARBAMOL	500 mg/1	60 TABLET, COATED in 1 BOTTLE (68071-4520-6)
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)
51655-195-84	51655-195	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20221116	N/A	ANDA	ANDA209312	Northwind Pharmaceuticals, LLC	METHOCARBAMOL	500 mg/1	14 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-195-84)
50090-3557-1	50090-3557	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180827	N/A	ANDA	ANDA209312	A-S Medication Solutions	METHOCARBAMOL	500 mg/1	20 TABLET, COATED in 1 BOTTLE (50090-3557-1)
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)
50090-3756-0	50090-3756	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20181031	N/A	ANDA	ANDA209312	A-S Medication Solutions	METHOCARBAMOL	500 mg/1	40 TABLET, COATED in 1 BOTTLE (50090-3756-0)
70518-1723-3	70518-1723	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20220512	N/A	ANDA	ANDA209312	REMEDYREPACK INC.	METHOCARBAMOL	500 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-3)
70518-1723-4	70518-1723	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20221017	N/A	ANDA	ANDA209312	REMEDYREPACK INC.	METHOCARBAMOL	500 mg/1	30 TABLET, COATED in 1 BLISTER PACK (70518-1723-4)
70518-1723-6	70518-1723	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20241224	N/A	ANDA	ANDA209312	REMEDYREPACK INC.	METHOCARBAMOL	500 mg/1	60 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-6)
70518-1723-7	70518-1723	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20250117	N/A	ANDA	ANDA209312	REMEDYREPACK INC.	METHOCARBAMOL	500 mg/1	90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-7)
70518-1723-8	70518-1723	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20250325	N/A	ANDA	ANDA209312	REMEDYREPACK INC.	METHOCARBAMOL	500 mg/1	15 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-8)
70518-1723-9	70518-1723	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20251013	N/A	ANDA	ANDA209312	REMEDYREPACK INC.	METHOCARBAMOL	500 mg/1	40 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1723-9)