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
51285-369-01	51285-369	HUMAN PRESCRIPTION DRUG	Trexall	Methotrexate	TABLET, FILM COATED	ORAL	20010503	N/A	ANDA	ANDA040385	Teva Women's Health, Inc.	METHOTREXATE SODIUM	15 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (51285-369-01)
51285-368-01	51285-368	HUMAN PRESCRIPTION DRUG	Trexall	Methotrexate	TABLET, FILM COATED	ORAL	20010503	N/A	ANDA	ANDA040385	Teva Women's Health, Inc.	METHOTREXATE SODIUM	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (51285-368-01)
51285-366-01	51285-366	HUMAN PRESCRIPTION DRUG	Trexall	Methotrexate	TABLET, FILM COATED	ORAL	20010503	N/A	ANDA	ANDA040385	Teva Women's Health, Inc.	METHOTREXATE SODIUM	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (51285-366-01)
51285-367-01	51285-367	HUMAN PRESCRIPTION DRUG	Trexall	Methotrexate	TABLET, FILM COATED	ORAL	20010503	N/A	ANDA	ANDA040385	Teva Women's Health, Inc.	METHOTREXATE SODIUM	7.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (51285-367-01)