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
63629-8576-1	63629-8576	HUMAN PRESCRIPTION DRUG	Linezolid	Linezolid	TABLET, FILM COATED	ORAL	20211216	N/A	ANDA	ANDA204239	Bryant Ranch Prepack	LINEZOLID	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (63629-8576-1)
31722-749-01	31722-749	HUMAN PRESCRIPTION DRUG	Linezolid	Linezolid	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA204239	Camber Pharmaceuticals, Inc.	LINEZOLID	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (31722-749-01)
31722-749-20	31722-749	HUMAN PRESCRIPTION DRUG	Linezolid	Linezolid	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA204239	Camber Pharmaceuticals, Inc.	LINEZOLID	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (31722-749-20)
31722-749-30	31722-749	HUMAN PRESCRIPTION DRUG	Linezolid	Linezolid	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA204239	Camber Pharmaceuticals, Inc.	LINEZOLID	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-749-30)
31722-749-31	31722-749	HUMAN PRESCRIPTION DRUG	Linezolid	Linezolid	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA204239	Camber Pharmaceuticals, Inc.	LINEZOLID	600 mg/1	150 TABLET, FILM COATED in 1 CARTON (31722-749-31)
60687-309-21	60687-309	HUMAN PRESCRIPTION DRUG	Linezolid	Linezolid	TABLET, FILM COATED	ORAL	20180207	N/A	ANDA	ANDA204239	American Health Packaging	LINEZOLID	600 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-309-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-309-11)