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=ANDA211298"
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
82804-042-30 82804-042 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20231218 N/A ANDA ANDA211298 Proficient Rx LP TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-042-30)
82804-042-60 82804-042 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20231218 N/A ANDA ANDA211298 Proficient Rx LP TADALAFIL 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (82804-042-60)
82804-040-60 82804-040 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20231110 N/A ANDA ANDA211298 Proficient Rx LP TADALAFIL 5 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (82804-040-60)
82804-040-90 82804-040 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20231110 N/A ANDA ANDA211298 Proficient Rx LP TADALAFIL 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82804-040-90)
82804-041-30 82804-041 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20231213 N/A ANDA ANDA211298 Proficient Rx LP TADALAFIL 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-041-30)
82804-042-90 82804-042 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20231218 N/A ANDA ANDA211298 Proficient Rx LP TADALAFIL 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82804-042-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase