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=ANDA203512"
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
43063-974-90 43063-974 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20190426 N/A ANDA ANDA203512 PD-Rx Pharmaceuticals, Inc. SPIRONOLACTONE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-974-90)
16729-225-16 16729-225 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170602 N/A ANDA ANDA203512 Accord Healthcare, Inc. SPIRONOLACTONE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (16729-225-16)
16729-225-17 16729-225 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170615 N/A ANDA ANDA203512 Accord Healthcare, Inc. SPIRONOLACTONE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (16729-225-17)
16729-226-01 16729-226 HUMAN PRESCRIPTION DRUG Spironolactone spironolactone TABLET, FILM COATED ORAL 20170602 N/A ANDA ANDA203512 Accord Healthcare, Inc. SPIRONOLACTONE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (16729-226-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase