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
76420-893-01	76420-893	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20250128	N/A	ANDA	ANDA209312	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	100 TABLET, COATED in 1 BOTTLE (76420-893-01)
76420-893-05	76420-893	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20250128	N/A	ANDA	ANDA209312	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	500 TABLET, COATED in 1 BOTTLE (76420-893-05)
76420-893-12	76420-893	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20250128	N/A	ANDA	ANDA209312	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	120 TABLET, COATED in 1 BOTTLE (76420-893-12)
76420-893-30	76420-893	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20250128	N/A	ANDA	ANDA209312	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	30 TABLET, COATED in 1 BOTTLE (76420-893-30)
76420-893-60	76420-893	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20250128	N/A	ANDA	ANDA209312	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	60 TABLET, COATED in 1 BOTTLE (76420-893-60)
76420-893-90	76420-893	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20250128	N/A	ANDA	ANDA209312	Asclemed USA, Inc.	METHOCARBAMOL	500 mg/1	90 TABLET, COATED in 1 BOTTLE (76420-893-90)
62207-770-41	62207-770	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180515	N/A	ANDA	ANDA209312	Granules India Ltd	METHOCARBAMOL	750 mg/1	24 TABLET, COATED in 1 BOTTLE (62207-770-41)
62207-770-43	62207-770	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180515	N/A	ANDA	ANDA209312	Granules India Ltd	METHOCARBAMOL	750 mg/1	100 TABLET, COATED in 1 BOTTLE (62207-770-43)
62207-770-47	62207-770	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180515	N/A	ANDA	ANDA209312	Granules India Ltd	METHOCARBAMOL	750 mg/1	500 TABLET, COATED in 1 BOTTLE (62207-770-47)
62207-770-49	62207-770	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180515	N/A	ANDA	ANDA209312	Granules India Ltd	METHOCARBAMOL	750 mg/1	1000 TABLET, COATED in 1 BOTTLE (62207-770-49)
51655-205-20	51655-205	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20230108	N/A	ANDA	ANDA209312	Northwind Pharmaceuticals, 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 Pharmaceuticals, LLC	METHOCARBAMOL	750 mg/1	30 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-205-52)
62207-754-41	62207-754	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180515	N/A	ANDA	ANDA209312	Granules India Ltd	METHOCARBAMOL	500 mg/1	24 TABLET, COATED in 1 BOTTLE (62207-754-41)
62207-754-43	62207-754	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180515	N/A	ANDA	ANDA209312	Granules India Ltd	METHOCARBAMOL	500 mg/1	100 TABLET, COATED in 1 BOTTLE (62207-754-43)
62207-754-47	62207-754	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180515	N/A	ANDA	ANDA209312	Granules India Ltd	METHOCARBAMOL	500 mg/1	500 TABLET, COATED in 1 BOTTLE (62207-754-47)
62207-754-49	62207-754	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol Tablets	TABLET, COATED	ORAL	20180515	N/A	ANDA	ANDA209312	Granules India Ltd	METHOCARBAMOL	500 mg/1	1000 TABLET, COATED in 1 BOTTLE (62207-754-49)
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)