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=ANDA209250"
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
71335-2583-5 71335-2583 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250403 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2583-5)
71335-2583-6 71335-2583 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250403 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 20 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2583-6)
71335-2583-7 71335-2583 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250403 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 20 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-2583-7)
71335-2583-8 71335-2583 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250403 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2583-8)
71335-2583-4 71335-2583 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250403 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 20 mg/1 5 TABLET, FILM COATED in 1 BOTTLE (71335-2583-4)
71335-2583-1 71335-2583 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250403 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2583-1)
71335-2583-2 71335-2583 HUMAN PRESCRIPTION DRUG tadalafil tadalafil TABLET, FILM COATED ORAL 20250403 N/A ANDA ANDA209250 Bryant Ranch Prepack TADALAFIL 20 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-2583-2)
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