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=NDA205435"
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
72000-310-06 72000-310 HUMAN PRESCRIPTION DRUG SIVEXTRO tedizolid phosphate TABLET, FILM COATED ORAL 20140620 N/A NDA NDA205435 Nabriva Therapeutics US, Inc. TEDIZOLID PHOSPHATE 200 mg/1 1 BLISTER PACK in 1 CARTON (72000-310-06) / 6 TABLET, FILM COATED in 1 BLISTER PACK
72000-310-30 72000-310 HUMAN PRESCRIPTION DRUG SIVEXTRO tedizolid phosphate TABLET, FILM COATED ORAL 20140620 N/A NDA NDA205435 Nabriva Therapeutics US, Inc. TEDIZOLID PHOSPHATE 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72000-310-30)
67919-041-04 67919-041 HUMAN PRESCRIPTION DRUG SIVEXTRO tedizolid phosphate TABLET, FILM COATED ORAL 20140620 N/A NDA NDA205435 Merck Sharp & Dohme LLC TEDIZOLID PHOSPHATE 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67919-041-04)
67919-041-05 67919-041 HUMAN PRESCRIPTION DRUG SIVEXTRO tedizolid phosphate TABLET, FILM COATED ORAL 20140620 N/A NDA NDA205435 Merck Sharp & Dohme LLC TEDIZOLID PHOSPHATE 200 mg/1 1 BLISTER PACK in 1 CARTON (67919-041-05) / 6 TABLET, FILM COATED in 1 BLISTER PACK
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