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）
检索条件:" 注册申请号=NDA021130"
符合检索条件的记录共 4 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
0009-5138-02 0009-5138 HUMAN PRESCRIPTION DRUG Zyvox linezolid TABLET, FILM COATED ORAL 20151012 N/A NDA NDA021130 Pharmacia & Upjohn Company LLC LINEZOLID 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (0009-5138-02)
0009-5138-03 0009-5138 HUMAN PRESCRIPTION DRUG Zyvox linezolid TABLET, FILM COATED ORAL 20151012 N/A NDA NDA021130 Pharmacia & Upjohn Company LLC LINEZOLID 600 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (0009-5138-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK
59762-1307-1 59762-1307 HUMAN PRESCRIPTION DRUG Linezolid linezolid TABLET, FILM COATED ORAL 20151012 N/A NDA AUTHORIZED GENERIC NDA021130 Greenstone LLC LINEZOLID 600 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (59762-1307-1)
59762-1307-2 59762-1307 HUMAN PRESCRIPTION DRUG Linezolid linezolid TABLET, FILM COATED ORAL 20151012 N/A NDA AUTHORIZED GENERIC NDA021130 Greenstone LLC LINEZOLID 600 mg/1 20 BLISTER PACK in 1 BOX, UNIT-DOSE (59762-1307-2) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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