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=NDA022127"
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
58468-0130-1 58468-0130 HUMAN PRESCRIPTION DRUG Renvela SEVELAMER CARBONATE TABLET, FILM COATED ORAL 20090812 N/A NDA NDA022127 Genzyme Corporation SEVELAMER CARBONATE 800 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (58468-0130-1)
58468-0133-1 58468-0133 HUMAN PRESCRIPTION DRUG Renvela SEVELAMER CARBONATE TABLET, FILM COATED ORAL 20230714 N/A NDA NDA022127 Genzyme Corporation SEVELAMER CARBONATE 800 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (58468-0133-1)
70518-2490-1 70518-2490 HUMAN PRESCRIPTION DRUG Sevelamer Carbonate Sevelamer Carbonate TABLET, FILM COATED ORAL 20230901 N/A NDA AUTHORIZED GENERIC NDA022127 REMEDYREPACK INC. SEVELAMER CARBONATE 800 mg/1 90 POUCH in 1 BOX (70518-2490-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2490-2)
0955-1057-30 0955-1057 HUMAN PRESCRIPTION DRUG Sevelamer Carbonate Sevelamer Carbonate TABLET, FILM COATED ORAL 20230714 N/A NDA AUTHORIZED GENERIC NDA022127 Winthrop U.S, a business of sanofi-aventis U.S. LLC SEVELAMER CARBONATE 800 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (0955-1057-30)
0955-1050-27 0955-1050 HUMAN PRESCRIPTION DRUG Sevelamer Carbonate Sevelamer Carbonate TABLET, FILM COATED ORAL 20180201 N/A NDA AUTHORIZED GENERIC NDA022127 Winthrop U.S, a business of sanofi-aventis U.S. LLC SEVELAMER CARBONATE 800 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (0955-1050-27)
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