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=ANDA209267"
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
31722-265-30 31722-265 HUMAN PRESCRIPTION DRUG ERLOTINIB ERLOTINIB TABLET, FILM COATED ORAL 20240524 N/A ANDA ANDA209267 Camber Pharmaceuticals, Inc. ERLOTINIB HYDROCHLORIDE 150 mg/1 1 BOTTLE in 1 CARTON (31722-265-30) / 30 TABLET, FILM COATED in 1 BOTTLE
31722-264-30 31722-264 HUMAN PRESCRIPTION DRUG ERLOTINIB ERLOTINIB TABLET, FILM COATED ORAL 20240524 N/A ANDA ANDA209267 Camber Pharmaceuticals, Inc. ERLOTINIB HYDROCHLORIDE 100 mg/1 1 BOTTLE in 1 CARTON (31722-264-30) / 30 TABLET, FILM COATED in 1 BOTTLE
31722-263-30 31722-263 HUMAN PRESCRIPTION DRUG ERLOTINIB ERLOTINIB TABLET, FILM COATED ORAL 20240524 N/A ANDA ANDA209267 Camber Pharmaceuticals, Inc. ERLOTINIB HYDROCHLORIDE 25 mg/1 1 BOTTLE in 1 CARTON (31722-263-30) / 30 TABLET, FILM COATED in 1 BOTTLE
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