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
85477-101-10	85477-101	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20251120	N/A	ANDA	ANDA200958	Oncora Pharma, LLC	METHOCARBAMOL	1000 mg/1	100 TABLET, COATED in 1 BOTTLE, PLASTIC (85477-101-10)
73352-510-10	73352-510	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20250210	N/A	ANDA	ANDA200958	Trifluent Pharma LLC	METHOCARBAMOL	1000 mg/1	100 TABLET, COATED in 1 BOTTLE (73352-510-10)
35561-212-12	35561-212	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20181010	N/A	ANDA	ANDA200958	AustarPharma LLC	METHOCARBAMOL	500 mg/1	100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-12)
35561-212-13	35561-212	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20181010	N/A	ANDA	ANDA200958	AustarPharma LLC	METHOCARBAMOL	500 mg/1	500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-212-13)
35561-211-12	35561-211	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20181009	N/A	ANDA	ANDA200958	AustarPharma LLC	METHOCARBAMOL	750 mg/1	100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-211-12)
35561-211-13	35561-211	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20181009	N/A	ANDA	ANDA200958	AustarPharma LLC	METHOCARBAMOL	750 mg/1	500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-211-13)
0276-0510-10	0276-0510	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20220913	N/A	ANDA	ANDA200958	Misemer Pharmaceutical	METHOCARBAMOL	1000 mg/1	100 TABLET, COATED in 1 BOTTLE, PLASTIC (0276-0510-10)
35561-349-12	35561-349	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20220716	N/A	ANDA	ANDA200958	AustarPharma LLC	METHOCARBAMOL	1000 mg/1	100 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-349-12)
35561-349-13	35561-349	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET, COATED	ORAL	20220716	N/A	ANDA	ANDA200958	AustarPharma LLC	METHOCARBAMOL	1000 mg/1	500 TABLET, COATED in 1 BOTTLE, PLASTIC (35561-349-13)