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
71335-2305-6	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20231116	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	90 TABLET in 1 BOTTLE (71335-2305-6)
71335-2305-7	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240403	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	112 TABLET in 1 BOTTLE (71335-2305-7)
71335-2305-8	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240403	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	21 TABLET in 1 BOTTLE (71335-2305-8)
71335-2305-9	71335-2305	HUMAN PRESCRIPTION DRUG	Methocarbamol	methocarbamol	TABLET	ORAL	20240403	N/A	ANDA	ANDA040489	Bryant Ranch Prepack	METHOCARBAMOL	750 mg/1	84 TABLET in 1 BOTTLE (71335-2305-9)
80425-0283-1	80425-0283	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20230307	N/A	ANDA	ANDA040489	Advanced Rx Pharmacy of Tennessee, LLC	METHOCARBAMOL	500 mg/1	30 TABLET in 1 BOTTLE (80425-0283-1)
80425-0283-2	80425-0283	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20230307	N/A	ANDA	ANDA040489	Advanced Rx Pharmacy of Tennessee, LLC	METHOCARBAMOL	500 mg/1	60 TABLET in 1 BOTTLE (80425-0283-2)
80425-0283-3	80425-0283	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20230307	N/A	ANDA	ANDA040489	Advanced Rx Pharmacy of Tennessee, LLC	METHOCARBAMOL	500 mg/1	90 TABLET in 1 BOTTLE (80425-0283-3)
80425-0283-4	80425-0283	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20230307	N/A	ANDA	ANDA040489	Advanced Rx Pharmacy of Tennessee, LLC	METHOCARBAMOL	500 mg/1	120 TABLET in 1 BOTTLE (80425-0283-4)
80425-0283-5	80425-0283	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20230307	N/A	ANDA	ANDA040489	Advanced Rx Pharmacy of Tennessee, LLC	METHOCARBAMOL	500 mg/1	180 TABLET in 1 BOTTLE (80425-0283-5)