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
50268-521-15	50268-521	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20210323	N/A	ANDA	ANDA090200	AvPAK	METHOCARBAMOL	750 mg/1	50 BLISTER PACK in 1 BOX (50268-521-15) / 1 TABLET in 1 BLISTER PACK (50268-521-11)
55154-2129-0	55154-2129	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20200325	N/A	ANDA	ANDA090200	Cardinal Health 107, LLC	METHOCARBAMOL	500 mg/1	10 BLISTER PACK in 1 BAG (55154-2129-0) / 1 TABLET in 1 BLISTER PACK
55154-2130-0	55154-2130	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20200325	N/A	ANDA	ANDA090200	Cardinal Health 107, LLC	METHOCARBAMOL	750 mg/1	10 BLISTER PACK in 1 BAG (55154-2130-0) / 1 TABLET in 1 BLISTER PACK
61919-368-07	61919-368	HUMAN PRESCRIPTION DRUG	METHOCARBAMOL	METHOCARBAMOL	TABLET	ORAL	20190418	N/A	ANDA	ANDA090200	DIRECT RX	METHOCARBAMOL	500 mg/1	7 TABLET in 1 BOTTLE (61919-368-07)
61919-368-30	61919-368	HUMAN PRESCRIPTION DRUG	METHOCARBAMOL	METHOCARBAMOL	TABLET	ORAL	20190418	N/A	ANDA	ANDA090200	DIRECT RX	METHOCARBAMOL	500 mg/1	30 TABLET in 1 BOTTLE (61919-368-30)
61919-368-40	61919-368	HUMAN PRESCRIPTION DRUG	METHOCARBAMOL	METHOCARBAMOL	TABLET	ORAL	20190418	N/A	ANDA	ANDA090200	DIRECT RX	METHOCARBAMOL	500 mg/1	40 TABLET in 1 BOTTLE (61919-368-40)
61919-368-60	61919-368	HUMAN PRESCRIPTION DRUG	METHOCARBAMOL	METHOCARBAMOL	TABLET	ORAL	20190418	N/A	ANDA	ANDA090200	DIRECT RX	METHOCARBAMOL	500 mg/1	60 TABLET in 1 BOTTLE (61919-368-60)
61919-368-90	61919-368	HUMAN PRESCRIPTION DRUG	METHOCARBAMOL	METHOCARBAMOL	TABLET	ORAL	20190418	N/A	ANDA	ANDA090200	DIRECT RX	METHOCARBAMOL	500 mg/1	90 TABLET in 1 BOTTLE (61919-368-90)
67046-1147-3	67046-1147	HUMAN PRESCRIPTION DRUG	Methocarbamol	Methocarbamol	TABLET	ORAL	20250130	N/A	ANDA	ANDA090200	Coupler LLC	METHOCARBAMOL	750 mg/1	30 TABLET in 1 BLISTER PACK (67046-1147-3)