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=NDA212018"
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
59676-050-28 59676-050 HUMAN PRESCRIPTION DRUG BALVERSA Erdafitinib TABLET, FILM COATED ORAL 20190412 N/A NDA NDA212018 Janssen Products LP ERDAFITINIB 5 mg/1 1 BOTTLE in 1 CARTON (59676-050-28) / 28 TABLET, FILM COATED in 1 BOTTLE
59676-030-56 59676-030 HUMAN PRESCRIPTION DRUG BALVERSA Erdafitinib TABLET, FILM COATED ORAL 20190412 N/A NDA NDA212018 Janssen Products LP ERDAFITINIB 3 mg/1 1 BOTTLE in 1 CARTON (59676-030-56) / 56 TABLET, FILM COATED in 1 BOTTLE
59676-030-84 59676-030 HUMAN PRESCRIPTION DRUG BALVERSA Erdafitinib TABLET, FILM COATED ORAL 20190412 N/A NDA NDA212018 Janssen Products LP ERDAFITINIB 3 mg/1 1 BOTTLE in 1 CARTON (59676-030-84) / 84 TABLET, FILM COATED in 1 BOTTLE
59676-040-28 59676-040 HUMAN PRESCRIPTION DRUG BALVERSA Erdafitinib TABLET, FILM COATED ORAL 20190412 N/A NDA NDA212018 Janssen Products LP ERDAFITINIB 4 mg/1 1 BOTTLE in 1 CARTON (59676-040-28) / 28 TABLET, FILM COATED in 1 BOTTLE
59676-040-56 59676-040 HUMAN PRESCRIPTION DRUG BALVERSA Erdafitinib TABLET, FILM COATED ORAL 20190412 N/A NDA NDA212018 Janssen Products LP ERDAFITINIB 4 mg/1 1 BOTTLE in 1 CARTON (59676-040-56) / 56 TABLET, FILM COATED in 1 BOTTLE
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