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
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)
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)
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)
50090-3756-0	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)
70934-756-30	70934-756	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20220503	20260331	ANDA	ANDA209312	Denton Pharma, Inc. dba Northwind Pharmaceuticals	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (70934-756-30)
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)
51655-205-52	51655-205	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20230413	N/A	ANDA	ANDA209312	Northwind Pharmaceuticals, LLC	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-205-52)
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)
63739-992-10	63739-992	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20210722	20260331	ANDA	ANDA209312	McKesson Corporation dba SKY Packaging	METHOCARBAMOL	750 mg/1	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-992-10) / 10 TABLET, COATED in 1 BLISTER PACK
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)
70518-1738-4	70518-1738	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20220429	N/A	ANDA	ANDA209312	REMEDYREPACK INC.	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BLISTER PACK (70518-1738-4)
70518-1738-5	70518-1738	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20220524	N/A	ANDA	ANDA209312	REMEDYREPACK INC.	METHOCARBAMOL	750 mg/1	20 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1738-5)